NDC Product
Human Prescription DrugCreon NDC 0032-1203
- Generic Name
- Pancrelipase
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- BLA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Triethyl Citrate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 8Z96QXD6UM.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 77-93-0 and the RxNorm Concept ID (RxCUI) 1310554. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
TRIETHYL CITRATE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
8Z96QXD6UM
The specific atomic composition represented as a molecular structure string.
InChIKey
C12H20O7 International Chemical Identifier digital signature for unique molecular identification.
SMILES String
DOOTYTYQINUNNV-UHFFFAOYSA-N Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
C(CC(=O)OCC)(CC(=O)OCC)(C(=O)OCC)O
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Triethyl Citrate. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.
FDA Official Name
TRIETHYL CITRATE
OF
Common Names & Synonyms
1,2,3-PROPANETRICARBOXYLIC ACID, 2-HYDROXY-, TRIETHYL ESTER
CN
CITRIC ACID ETHYL ESTER [MI]
CN
CITRIC ACID, TRIETHYL ESTER
CN
TRIETHYL CITRATE [EP MONOGRAPH]
CN
TRIETHYL CITRATE [FCC]
CN
TRIETHYL CITRATE [FHFI]
CN
TRIETHYL CITRATE [HSDB]
CN
TRIETHYL CITRATE [II]
CN
TRIETHYL CITRATE [MART.]
CN
TRIETHYL CITRATE [USP-RS]
CN
Brand / Trade Names
CITROFLEX 2
BN
CITROFLEX C 2
BN
CITROFLEX EC
BN
CITROFLEX SC 60
BN
CITROFOL AI
BN
EUDRAFLEX
BN
HYDRAGEN CAT
BN
MORFLEX C 2
BN
MORFLEX TEC
BN
Systematic Nomenclature
CITRIC ACID ETHYL ESTER
SYS
ETHYL CITRATE
SYS
Technical Codes
E-1505
CD
FEMA NO. 3083
CD
INS NO.1505
CD
INS-1505
CD
NSC-8907
CD
NDC Products Containing TRIETHYL CITRATE
This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory:
Manufacturer Quick Index
Note: Due to the high number of listings (500), only Active Listings are currently displayed. Display is limited to the first 200 products.
Showing 200 active products
AbbVie Inc.
Active Listing
NDC Product
Human Prescription DrugCreon NDC 0032-1206
- Generic Name
- Pancrelipase
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugCreon NDC 0032-1212
- Generic Name
- Pancrelipase
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugCreon NDC 0032-1224
- Generic Name
- Pancrelipase
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugCreon NDC 0032-3016
- Generic Name
- Pancrelipase
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugDepakote Sprinkles NDC 0074-6114
- Generic Name
- Divalproex Sodium
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Actavis Pharma, Inc.
NDC Product
Human Prescription DrugLamotrigine NDC 0228-1422
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLamotrigine NDC 0228-1453
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLamotrigine NDC 0228-1580
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLamotrigine NDC 0228-1638
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Fluvoxamine Maleate
- Dosage Form
- Capsule, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugFluvoxamine Maleate NDC 0228-2848
- Generic Name
- Fluvoxamine Maleate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFluvoxamine Maleate NDC 0228-2849
- Generic Name
- Fluvoxamine Maleate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Fluvoxamine Maleate
- Dosage Form
- Capsule, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 0228-2890
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 0228-2891
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugDuloxetine NDC 0228-2892
- Generic Name
- Duloxetine
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 0228-2918
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate NDC 0228-3059
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate NDC 0228-3060
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate NDC 0228-3061
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate NDC 0228-3062
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate NDC 0228-3063
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate NDC 0228-3064
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Allergan, Inc.
NDC Product
Human Prescription DrugAtelvia NDC 0430-0979
- Generic Name
- Risedronate Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFetzima NDC 0456-2202
- Generic Name
- Levomilnacipran Hydrochloride
- Dosage Form
- Kit
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFetzima NDC 0456-2212
- Generic Name
- Levomilnacipran Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFetzima NDC 0456-2220
- Generic Name
- Levomilnacipran Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFetzima NDC 0456-2240
- Generic Name
- Levomilnacipran Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugFetzima NDC 0456-2280
- Generic Name
- Levomilnacipran Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Almay, Inc.
NDC Product
Human Otc Drug- Generic Name
- Titanium Dioxide, Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Titanium Dioxide, Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Titanium Dioxide, Zinc Oxide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Amneal Pharmaceuticals of New York LLC
NDC Product
Human Prescription DrugCarvedilol Phosphate NDC 0115-1248
- Generic Name
- Carvedilol Phosphate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarvedilol Phosphate NDC 0115-1249
- Generic Name
- Carvedilol Phosphate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarvedilol Phosphate NDC 0115-1250
- Generic Name
- Carvedilol Phosphate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCarvedilol Phosphate NDC 0115-1251
- Generic Name
- Carvedilol Phosphate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 0115-1486
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 0115-1487
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 0115-1488
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 0115-1489
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 0115-1490
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 0115-1491
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
AstraZeneca Pharmaceuticals LP
NDC Product
Human Prescription DrugNexium NDC 0186-4010
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-4020
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-4025
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-4040
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-4050
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-5020
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNexium NDC 0186-5040
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Bausch Health US LLC
NDC Product
Human Prescription DrugWellbutrin Xl NDC 0187-0730
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugWellbutrin Xl NDC 0187-0731
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
Bayer HealthCare LLC.
NDC Product
Human Otc DrugBayer Low Dose NDC 0280-2100
- Generic Name
- Aspirin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBayer Aspirin Regimen Enteric Coated NDC 0280-2110
- Generic Name
- Aspirin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
C.B. Fleet Company, Inc.
NDC Product
Human Otc DrugFleet NDC 0132-0401
- Generic Name
- Bisacodyl
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Crown Laboratories
NDC Product
Human Otc DrugBlue Lizard Sheer Spf 50 Sunscreen NDC 0316-2059
- Generic Name
- Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugBlue Lizard Sheer Spf 50 Sunscreen NDC 0316-2064
- Generic Name
- Titanium Dioxide, Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Crown Laboratories, Inc.
NDC Product
Human Otc DrugDesenex Antifungal Foot Cream NDC 0316-0255
- Generic Name
- Miconazole Nitrate
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Galderma Laboratories, L.P.
NDC Product
Human Prescription DrugOracea NDC 0299-3822
- Generic Name
- Doxycycline
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
GlaxoSmithKline LLC
NDC Product
Human Prescription DrugLamictal Xr NDC 0173-0754
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLamictal Xr NDC 0173-0755
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLamictal Xr NDC 0173-0756
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLamictal Xr NDC 0173-0757
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLamictal Xr NDC 0173-0758
- Generic Name
- Lamotrigine
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLamictal Xr NDC 0173-0759
- Generic Name
- Lamotrigine
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLamictal Xr NDC 0173-0760
- Generic Name
- Lamotrigine
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLamictal Xr NDC 0173-0761
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLamictal Xr NDC 0173-0781
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- NDA
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugGood Sense Lansoprazole NDC 0113-0116
- Generic Name
- Lansoprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugGood Sense Omeprazole NDC 0113-0520
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugGood Sense Esomeprazole Magnesium NDC 0113-0651
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Esomeprazole Magnesium NDC 0113-0898
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Omeprazole NDC 0113-0915
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugGood Sense Omeprazole NDC 0113-1723
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugGood Sense Omeprazole Delayed Release NDC 0113-1803
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugGood Sense Esomeprazole Magnesium NDC 0113-2022
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lannett Company Inc.
NDC Product
Human Prescription DrugMesalamine NDC 0527-3012
- Generic Name
- Mesalamine
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lannett Company, Inc.
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 0527-0790
- Generic Name
- Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amp...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 0527-0791
- Generic Name
- Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amp...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 0527-0792
- Generic Name
- Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amp...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 0527-0793
- Generic Name
- Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amp...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 0527-0794
- Generic Name
- Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amp...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate NDC 0527-0795
- Generic Name
- Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amp...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride Extended-release NDC 0527-8106
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride Extended-release NDC 0527-8107
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride Extended-release NDC 0527-8108
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride Extended-release NDC 0527-8109
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride Extended-release NDC 0527-8110
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride Extended-release NDC 0527-8111
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride Extended-release NDC 0527-8112
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride Extended-release NDC 0527-8113
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugMesalamine NDC 0378-1375
- Generic Name
- Mesalamine
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexlansoprazole NDC 0378-2085
- Generic Name
- Dexlansoprazole
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexlansoprazole NDC 0378-2086
- Generic Name
- Dexlansoprazole
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEsomeprazole Magnesium NDC 0378-2350
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEsomeprazole Magnesium NDC 0378-2351
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBudesonide NDC 0378-4500
- Generic Name
- Budesonide
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 0378-6001
- Generic Name
- Metformin
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMetformin Hydrochloride NDC 0378-6002
- Generic Name
- Metformin
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 0378-6688
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 0378-6689
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLansoprazole NDC 0378-6981
- Generic Name
- Lansoprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLansoprazole NDC 0378-6982
- Generic Name
- Lansoprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugKetoprofen NDC 0378-8200
- Generic Name
- Ketoprofen
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugArthrotec NDC 0025-1411
- Generic Name
- Diclofenac Sodium And Misoprostol
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugArthrotec NDC 0025-1421
- Generic Name
- Diclofenac Sodium And Misoprostol
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
SpecGx LLC
NDC Product
Human Prescription DrugMixed Salts Of A Single-entity Amphetamine Product NDC 0406-0803
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single-entity Amphetamine Product NDC 0406-0804
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single-entity Amphetamine Product NDC 0406-0805
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single-entity Amphetamine Product NDC 0406-0807
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single Entity Amphetamine Product Xr NDC 0406-8951
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single Entity Amphetamine Product Xr NDC 0406-8952
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single Entity Amphetamine Product Xr NDC 0406-8953
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single Entity Amphetamine Product Xr NDC 0406-8954
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single Entity Amphetamine Product Xr NDC 0406-8955
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMixed Salts Of A Single Entity Amphetamine Product Xr NDC 0406-8956
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugLansoprazole NDC 0093-3008
- Generic Name
- Lansoprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLansoprazole NDC 0093-3009
- Generic Name
- Lansoprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5045
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5046
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 0093-5346
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 0093-5347
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride (la) NDC 0093-5348
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5550
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5551
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5552
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5553
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5554
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexmethylphenidate Hydrochloride NDC 0093-5562
- Generic Name
- Dexmethylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 0093-7163
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugTolterodine Tartrate NDC 0093-7164
- Generic Name
- Tolterodine Tartrate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLansoprazole NDC 0093-7350
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLansoprazole NDC 0093-7351
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 0093-8192
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 0093-8204
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- N/A
- Marketing
- DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription DrugCimetidine NDC 0093-8305
- Generic Name
- Cimetidine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMesalamine NDC 0093-9224
- Generic Name
- Mesalamine
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Teva Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, And Amphetamine Sulfate NDC 0480-3683
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, And Amphetamine Sulfate NDC 0480-3684
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, And Amphetamine Sulfate NDC 0480-3685
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, And Amphetamine Sulfate NDC 0480-3686
- Generic Name
- Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydr...
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTiopronin NDC 0480-7824
- Generic Name
- Tiopronin
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTiopronin NDC 0480-9227
- Generic Name
- Tiopronin
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Upsher-Smith Laboratories, LLC
NDC Product
Human Prescription DrugKlor-con NDC 0245-0835
- Generic Name
- Potassium Chloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugKlor-con NDC 0245-0836
- Generic Name
- Potassium Chloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREEN CO.
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 0363-0361
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 0363-0508
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcid Reducer NDC 0363-1008
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREENS
NDC Product
Human Otc DrugLow Dose Aspirin NDC 0363-0686
- Generic Name
- Aspirin 81 Mg Delayed Release Tablets
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLow Dose Aspirin NDC 0363-0690
- Generic Name
- Aspirin 81 Mg Delayed Release Tablets
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAspirin 81 NDC 0363-6452
- Generic Name
- Aspirin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAspirin 325 Mg NDC 0363-6453
- Generic Name
- Aspirin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDye-free Aspirin 81 NDC 0363-6455
- Generic Name
- Aspirin
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEsomeprazole Magnesium Delayed Release NDC 0363-7810
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
WALGREENS COMPANY
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 0363-0772
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreen Company
NDC Product
Human Otc DrugOmeprazole NDC 0363-0007
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAspirin Enteric Coated, Regular Strength NDC 0363-0227
- Generic Name
- Aspirin
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGentle Laxative NDC 0363-0327
- Generic Name
- Bisacodyl
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAspirin Enteric Coated Low Dose NDC 0363-0563
- Generic Name
- Aspirin
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAspirin NDC 0363-0587
- Generic Name
- Aspirin
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAspirin 325 NDC 0363-0691
- Generic Name
- Aspirin
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugOmeprazole NDC 0363-0915
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugWalgreens Pain Relief Plus Uti Bacteria Control NDC 0363-1277
- Generic Name
- Methenamine, Sodium Salicylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugLansoprazole NDC 0363-1419
- Generic Name
- Lansoprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 0363-1699
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugOmeprazole NDC 0363-1819
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Orally Disintegrating, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugOmeprazole NDC 0363-4099
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugWalgreens Antibacterial Plus Urinary Pain Relief NDC 0363-4404
- Generic Name
- Methenamine, Sodium Salicylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc DrugOmeprazole NDC 0363-6089
- Generic Name
- Omeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugOmeprazole NDC 0363-6101
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugAspirin Enteric Coated Low Dose NDC 0363-6450
- Generic Name
- Aspirin
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLaxative NDC 0363-6760
- Generic Name
- Bisacodyl
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 0363-7223
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugOmeprazole NDC 0363-9980
- Generic Name
- Omeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreens
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 0363-1353
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugOmeprazole NDC 0363-9510
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreens Company
NDC Product
Human Otc DrugOmeprazole Magnesium NDC 0363-0042
- Generic Name
- Omeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugOmeprazole NDC 0363-1607
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
NDC Product
Human Prescription DrugProtonix Delayed-release NDC 0008-0841
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugProtonix Delayed-release NDC 0008-0843
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugProtonix Delayed-release NDC 0008-0844
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPrempro NDC 0046-1105
- Generic Name
- Conjugated Estrogens And Medroxyprogesterone Acetate
- Dosage Form
- Tablet, Sugar Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPrempro NDC 0046-1106
- Generic Name
- Conjugated Estrogens And Medroxyprogesterone Acetate
- Dosage Form
- Tablet, Sugar Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPrempro NDC 0046-1107
- Generic Name
- Conjugated Estrogens And Medroxyprogesterone Acetate
- Dosage Form
- Tablet, Sugar Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPrempro NDC 0046-1108
- Generic Name
- Conjugated Estrogens And Medroxyprogesterone Acetate
- Dosage Form
- Tablet, Sugar Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPremphase NDC 0046-2575
- Generic Name
- Conjugated Estrogens And Medroxyprogesterone Acetate
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- NDA
Active Listing
