NDC Product
Human Otc DrugNaphcon A NDC 0065-0085
- Generic Name
- Naphazoline Hydrochloride And Pheniramine Maleate
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- NDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Edetate Disodium, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 7FLD91C86K.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 6381-92-6 and the RxNorm Concept ID (RxCUI) 1310470. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
EDETATE DISODIUM
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
7FLD91C86K
The specific atomic composition represented as a molecular structure string.
InChIKey
C10H14N2O8.2Na.2H2O International Chemical Identifier digital signature for unique molecular identification.
SMILES String
OVBJJZOQPCKUOR-UHFFFAOYSA-L 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
EDETATE DISODIUM
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
N(CC([O-])=O)(CC(=O)O)CCN(CC([O-])=O)CC(=O)O.[Na+].O.[Na+].O
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Edetate Disodium. 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.
Common Names & Synonyms
(ETHYLENEDINITRILO) TETRAACETIC ACID DISODIUM SALT DIHYDRATE
CN
DISODIUM EDETATE HYDRATE [JAN]
CN
DISODIUM EDETATE [EP IMPURITY]
CN
DISODIUM EDETATE [EP MONOGRAPH]
CN
DISODIUM EDETATE [WHO-IP]
CN
DISODIUM EDTA
CN
DISODIUM EDTA DIHYDRATE
CN
DISODIUM EDTA [FCC]
CN
DISODIUM EDTA [VANDF]
CN
Disodium edetate dihydrate [WHO-DD]
CN
E-386
CN
EDETATE DISODIUM [II]
CN
EDETATE DISODIUM [ORANGE BOOK]
CN
EDETATE DISODIUM [USP MONOGRAPH]
CN
EDETATE DISODIUM [USP-RS]
CN
EDETATE DISODIUM [VANDF]
CN
EDTA DISODIUM
CN
EDTA DISODIUM SALT
CN
GLYCINE, N,N'-1,2-ETHANEDIYLBIS N-(CARBOXYMETHYL)-, DISODIUM SALT, DIHYDRATE
CN
INS NO.386
CN
INS-386
CN
Brand / Trade Names
CHELEST F-NA
BN
Dissolvine NA2-P
BN
ENDRATE
BN
Edeta BD
BN
SODIUM VERSENATE
BN
TITRIPLEX III
BN
VERSENE NA2 Crystals
BN
Versene NA
BN
Systematic Nomenclature
DISODIUM EDETATE DIHYDRATE
SYS
DISODIUM EDETATE HYDRATE
SYS
DISODIUM ETHYLENEDIAMINETETRAACETATE
SYS
DISODIUM ETHYLENEDIAMINETETRAACETATE DIHYDRATE
SYS
Disodium (ethylenedinitrilo)tetraacetate dihydrate
SYS
EDETATE DISODIUM
SYS
EDETATE DISODIUM DIHYDRATE
SYS
Technical Codes
NSC-759604
CD
NDC Products Containing EDETATE DISODIUM
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
Alcon Laboratories, Inc.
Active Listing
NDC Product
Human Prescription DrugMydriacyl NDC 0065-0355
- Generic Name
- Tropicamide
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclomydril NDC 0065-0359
- Generic Name
- Cyclopentolate Hydrochloride And Phenylephrine Hydrochloride
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclogyl NDC 0065-0395
- Generic Name
- Cyclopentolate Hydrochloride
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclogyl NDC 0065-0396
- Generic Name
- Cyclopentolate Hydrochloride
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugCyclogyl NDC 0065-0397
- Generic Name
- Cyclopentolate Hydrochloride
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSystane NDC 0065-0454
- Generic Name
- Polyethylene Glycol 400 And Propylene Glycol
- Dosage Form
- Gel
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSystane Complete NDC 0065-0481
- Generic Name
- Propylene Glycol
- Dosage Form
- Emulsion
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSystane Balance NDC 0065-1433
- Generic Name
- Propylene Glycol
- Dosage Form
- Emulsion
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSystane Day And Night Value Pack NDC 0065-1502
- Generic Name
- Polyethylene Glycol 400, Propylene Glycol 0.3%
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGenteal Tears Gel Drops NDC 0065-8067
- Generic Name
- Polyethylene Glycol 400 And Propylene Glycol
- Dosage Form
- Gel
- Route
- Ophthalmic
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPataday Once Daily Relief NDC 0065-8150
- Generic Name
- Olopatadine Hydrochloride
- Dosage Form
- Solution
- Route
- Ophthalmic
- Marketing
- NDA
Active Listing
Allergan, Inc.
NDC Product
Human Otc DrugSkinmedica Acne Clarifying Treatment NDC 0023-1230
- Generic Name
- Salicylic Acid
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugAcular NDC 0023-2181
- Generic Name
- Ketorolac Tromethamine
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugZymaxid NDC 0023-3615
- Generic Name
- Gatifloxacin
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLastacaft NDC 0023-4290
- Generic Name
- Alcaftadine
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugLastacaft NDC 0023-4291
- Generic Name
- Alcaftadine
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugSkin Medica Purifying Foaming Wash NDC 0023-4948
- Generic Name
- Salicylic Acid
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTotal Defense Repair Broad Spectrum Spf 34 Sunscreen NDC 0023-5494
- Generic Name
- Octinoxate, Octisalate And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Octinoxate, Octisalate, Titanium Dioxide And Zinc Oxide
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Zinc Oxide And Octinoxate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugAcular Ls NDC 0023-9277
- Generic Name
- Ketorolac Tromethamine
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Marketing
- NDA
Active Listing
Amneal Pharmaceuticals of New York LLC
NDC Product
Human Prescription DrugBudesonide Inhalation NDC 0115-1687
- Generic Name
- Budesonide
- Dosage Form
- Suspension
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBudesonide Inhalation NDC 0115-1689
- Generic Name
- Budesonide
- Dosage Form
- Suspension
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevalbuterol NDC 0115-9930
- Generic Name
- Levalbuterol Hydrochloride
- Dosage Form
- Solution
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevalbuterol NDC 0115-9931
- Generic Name
- Levalbuterol Hydrochloride
- Dosage Form
- Solution
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevalbuterol NDC 0115-9932
- Generic Name
- Levalbuterol Hydrochloride
- Dosage Form
- Solution
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
AstraZeneca Pharmaceuticals LP
NDC Product
Human Prescription DrugPulmicort Respules NDC 0186-1988
- Generic Name
- Budesonide
- Dosage Form
- Suspension
- Route
- Respiratory (inhalation)
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPulmicort Respules NDC 0186-1989
- Generic Name
- Budesonide
- Dosage Form
- Suspension
- Route
- Respiratory (inhalation)
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugPulmicort Respules NDC 0186-1990
- Generic Name
- Budesonide
- Dosage Form
- Suspension
- Route
- Respiratory (inhalation)
- Marketing
- NDA
Active Listing
Bausch Health US LLC
NDC Product
Human Prescription DrugRetin-a Micro NDC 0187-5140
- Generic Name
- Tretinoin
- Dosage Form
- Gel
- Route
- Topical
- Marketing
- NDA
Active Listing
Bausch Health US, LLC
NDC Product
Human Prescription DrugBryhali NDC 0187-0002
- Generic Name
- Halobetasol Propionate
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugDuobrii NDC 0187-0653
- Generic Name
- Halobetasol Propionate And Tazarotene
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugArazlo NDC 0187-2098
- Generic Name
- Tazarotene
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugEfudex NDC 0187-3204
- Generic Name
- Fluorouracil
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- NDA
Active Listing
C.B. Fleet Company, Inc.
NDC Product
Human Otc DrugFleet NDC 0132-0075
- Generic Name
- Glycerin
- Dosage Form
- Suppository
- Route
- Rectal
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFleet NDC 0132-0078
- Generic Name
- Sodium Phosphate, Dibasic And Sodium Phosphate, Monobasic
- Dosage Form
- Enema
- Route
- Rectal
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPedia-lax NDC 0132-0113
- Generic Name
- Docusate Sodium
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFleet NDC 0132-0185
- Generic Name
- Glycerin
- Dosage Form
- Liquid
- Route
- Rectal
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPedia-lax NDC 0132-0190
- Generic Name
- Glycerin
- Dosage Form
- Liquid
- Route
- Rectal
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPedia-lax NDC 0132-0195
- Generic Name
- Glycerin
- Dosage Form
- Liquid
- Route
- Rectal
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFleet NDC 0132-0201
- Generic Name
- Sodium Phosphate, Dibasic And Sodium Phosphate, Monobasic
- Dosage Form
- Enema
- Route
- Rectal
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugPedia-lax NDC 0132-0202
- Generic Name
- Sodium Phosphate, Dibasic And Sodium Phosphate, Monobasic
- Dosage Form
- Enema
- Route
- Rectal
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC
NDC Product
Human Prescription DrugAdapalene NDC 0168-0424
- Generic Name
- Adapalene
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- ANDA
Active Listing
GlaxoSmithKline LLC
NDC Product
Human Prescription DrugBlenrep NDC 0173-0913
- Generic Name
- Belantamab Mafodotin
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intravenous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugExdensur NDC 0173-0927
- Generic Name
- Depemokimab
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
Haleon US Holdings LLC
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug- Generic Name
- Acetaminophen, Diphenhydramine Hcl
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Severe Multi-symptom Cough Cold Flu NDC 0031-8751
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, P...
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugRobitussin Severe Multi-symptom Cough Cold Flu Nighttime NDC 0031-8752
- Generic Name
- Acetaminophen, Diphenhydramine Hydrochloride, Phenylephrine ...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Chest Congestion Daytime NDC 0067-0104
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Guaifenesin
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief Nighttime NDC 0067-0105
- Generic Name
- Acetaminophen, Diphenhydramine Hcl
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Cold Relief NDC 0067-0107
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Diphenphydramine Hcl, G...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Congestion Relief Cooling Nasal Mist NDC 0067-0109
- Generic Name
- Oxymetazoline Hcl
- Dosage Form
- Spray
- Route
- Nasal
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Severe Congestion Relief Nasal Mist NDC 0067-0110
- Generic Name
- Oxymetazoline Hcl
- Dosage Form
- Spray
- Route
- Nasal
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugExcedrin Extra Strength Geltabs NDC 0067-2021
- Generic Name
- Acetaminophen, Asprin, Caffeine
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Daytime Nighttime Value Pack NDC 0067-8125
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl And A...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Daytime Severe Cold And Cough NDC 0067-8127
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Nighttime Severe Cold And Cough NDC 0067-8129
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugTheraflu Expressmax Severe Cold And Flu Syrup NDC 0067-8132
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephr...
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGaviscon NDC 0135-0094
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGaviscon NDC 0135-0095
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Intensive Enamel Repair Clean Mint NDC 0135-0449
- Generic Name
- Sodium Fluoride
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSensodyne Pronamel Intensive Enamel Repair Extra Fresh NDC 0135-0451
- Generic Name
- Sodium Fluoride
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGaviscon NDC 0135-0574
- Generic Name
- Aluminum Hydroxide And Magnesium Carbonate
- Dosage Form
- Liquid
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugFlonase Sensimist Allergy Relief NDC 0135-0615
- Generic Name
- Fluticasone Furoate
- Dosage Form
- Spray, Metered
- Route
- Nasal
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugFlonase Sensimist Allergy Relief NDC 0135-0616
- Generic Name
- Fluticasone Furoate
- Dosage Form
- Spray, Metered
- Route
- Nasal
- Marketing
- NDA
Active Listing
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0054-0517
- Generic Name
- Morphine Sulfate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugAminocaproic Acid NDC 0054-1100
- Generic Name
- Aminocaproic Acid
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugMidazolam Hydrochloride NDC 0054-3566
- Generic Name
- Midazolam Hydrochloride
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone Intensol NDC 0054-3721
- Generic Name
- Prednisone Intensol
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-3722
- Generic Name
- Prednisone
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropranolol Hydrochloride NDC 0054-3727
- Generic Name
- Propranolol Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropranolol Hydrochloride NDC 0054-3730
- Generic Name
- Propranolol Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-8724
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-8739
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisone NDC 0054-8740
- Generic Name
- Prednisone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGentamicin NDC 0143-9128
- Generic Name
- Gentamicin
- Dosage Form
- Injection, Solution
- Route
- Intramuscular; Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugGentamicin NDC 0143-9129
- Generic Name
- Gentamicin
- Dosage Form
- Injection, Solution
- Route
- Intramuscular; Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugStarjemza NDC 0143-9171
- Generic Name
- Ustekinumab-hmny
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugMesna NDC 0143-9260
- Generic Name
- Mesna
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClindamycin In 5 Percent Dextrose NDC 0143-9267
- Generic Name
- Clindamycin In Percent Dextrose
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClindamycin In 5 Percent Dextrose NDC 0143-9268
- Generic Name
- Clindamycin In 5 Percent Dextrose
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClindamycin In 5 Percent Dextrose NDC 0143-9269
- Generic Name
- Clindamycin In 5 Percent Dextrose
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLabetalol Hydrochloride NDC 0143-9320
- Generic Name
- Labetalol Hydrochloride
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLabetalol Hcl In Sodium Chloride NDC 0143-9363
- Generic Name
- Labetalol Hydrochloride
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLabetalol Hcl In Sodium Chloride NDC 0143-9364
- Generic Name
- Labetalol Hydrochloride
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLabetalol Hcl In Sodium Chloride NDC 0143-9365
- Generic Name
- Labetalol Hydrochloride
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugLabetalol Hcl In Dextrose NDC 0143-9366
- Generic Name
- Labetalol Hydrochloride
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugTerbutaline Sulfate NDC 0143-9375
- Generic Name
- Terbutaline Sulfate
- Dosage Form
- Injection
- Route
- Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFosaprepitant Dimeglumine NDC 0143-9384
- Generic Name
- Fosaprepitant Dimeglumine
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFosaprepitant Dimeglumine NDC 0143-9428
- Generic Name
- Fosaprepitant Dimeglumine
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLabetalol Hydrochloride NDC 0143-9622
- Generic Name
- Labetalol Hydrochloride
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLabetalol Hydrochloride NDC 0143-9623
- Generic Name
- Labetalol Hydrochloride
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugValproate Sodium NDC 0143-9637
- Generic Name
- Valproate Sodium
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFlumazenil NDC 0143-9683
- Generic Name
- Flumazenil
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFlumazenil NDC 0143-9684
- Generic Name
- Flumazenil
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTerbutaline Sulfate NDC 0143-9746
- Generic Name
- Terbutaline Sulfate
- Dosage Form
- Injection
- Route
- Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFlumazenil NDC 0143-9783
- Generic Name
- Flumazenil
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugFlumazenil NDC 0143-9784
- Generic Name
- Flumazenil
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugValproate Sodium NDC 0143-9785
- Generic Name
- Valproate Sodium
- Dosage Form
- Injection
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugDexamethasone Intensol NDC 0054-3176
- Generic Name
- Dexamethasone Intensol
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-3177
- Generic Name
- Dexamethasone
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8174
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8175
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8176
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8179
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8180
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8181
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDexamethasone NDC 0054-8183
- Generic Name
- Dexamethasone
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Hikma Pharmceuticals USA Inc.
NDC Product
Human Prescription DrugOxycodone Hydrochloride NDC 0054-0390
- Generic Name
- Oxycodone Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
L. Perrigo Company
NDC Product
Human Otc DrugGood Sense Severe Nighttime NDC 0113-0019
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate, P...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Nasal NDC 0113-0304
- Generic Name
- Oxymetazoline Hydrochloride
- Dosage Form
- Spray
- Route
- Nasal
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Nasal NDC 0113-0388
- Generic Name
- Oxymetazoline Hcl
- Dosage Form
- Spray
- Route
- Nasal
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Nasal Allergy NDC 0113-0443
- Generic Name
- Triamcinolone Acetonide
- Dosage Form
- Spray, Metered
- Route
- Nasal
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Severe Daytime Cold And Flu NDC 0113-0603
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephr...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Daytime Non Drowsy Cold And Flu NDC 0113-0656
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Allergy Relief NDC 0113-0671
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Severe Nighttime Cold And Flu NDC 0113-0763
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate, P...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Hemorrhoidal Maximum Strength Pain Relief NDC 0113-0944
- Generic Name
- Glycerin, Phenylephrine Hcl, Pramoxine Hcl, White Petrolatum
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Cold And Cough NDC 0113-0987
- Generic Name
- Brompheniramine Maleate, Dextromethorphan Hbr, Phenylephrine...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Allergy Relief NDC 0113-1719
- Generic Name
- Loratadine
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugGood Sense Tussin NDC 0113-2009
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Day Time Cold And Flu NDC 0113-2299
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, P...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Night Time Cold And Flu NDC 0113-2501
- Generic Name
- Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Suc...
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMederma Stretch Marks Therapy NDC 0113-4053
- Generic Name
- Dimethicone
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGoodsense Combo Pack Daytime And Nighttime NDC 0113-5970
- Generic Name
- Acetaminophen, Dextromethorphan Hbr, Doxylamine Succinate, G...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Childrens Cold Cough NDC 0113-6019
- Generic Name
- Brompheniramine Maleate, Dextromethorphan Hydrobromide
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGood Sense Nasal NDC 0113-6200
- Generic Name
- Oxymetazoline Hydrochloride
- Dosage Form
- Spray
- Route
- Nasal
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Liebel-Flarsheim Company LLC
NDC Product
Human Prescription DrugMd Gastroview NDC 0019-4816
- Generic Name
- Diatrizoate Meglumine And Diatrizoate Sodium
- Dosage Form
- Solution
- Route
- Oral; Rectal
- Marketing
- ANDA
Active Listing
Merck Sharp & Dohme LLC
NDC Product
Human Prescription DrugEmend NDC 0006-3061
- Generic Name
- Fosaprepitant Dimeglumine
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNoxafil NDC 0085-2224
- Generic Name
- Posaconazole
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugNoxafil NDC 0085-4331
- Generic Name
- Posaconazole
- Dosage Form
- Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
Mission Pharmacal Company
NDC Product
Human Prescription DrugAvar-e Green NDC 0178-0460
- Generic Name
- Sulfacetamide Sodium, Sulfur
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugAvar-e Ls NDC 0178-0465
- Generic Name
- Sulfacetamide Sodium, Sulfur
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugAvar-e NDC 0178-0470
- Generic Name
- Sulfacetamide Sodium, Sulfur
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugOvace Plus NDC 0178-0485
- Generic Name
- Sulfacetamide Sodium
- Dosage Form
- Shampoo
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugOvaceplus Plus NDC 0178-0495
- Generic Name
- Sulfacetamide Sodium
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugOvace Plus NDC 0178-0620
- Generic Name
- Sulfacetamide Sodium
- Dosage Form
- Lotion
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription DrugOvace Plus NDC 0178-0630
- Generic Name
- Sodium Sulfacetamide
- Dosage Form
- Liquid
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
PAI Holdings, LLC
NDC Product
Human Otc DrugGuaifenesin And Codeine Phosphate NDC 0121-0775
- Generic Name
- Guaifenesin And Codeine Phosphate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGuaifenesin And Codeine Phosphate NDC 0121-1550
- Generic Name
- Guaifenesin And Codeine Phosphate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugGuaifenesin And Codeine Phosphate NDC 0121-1775
- Generic Name
- Guaifenesin And Codeine Phosphate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
PAI Holdings, LLC dba PAI Pharma
NDC Product
Human Prescription DrugPrednisolone Sodium Phosphate NDC 0121-0759
- Generic Name
- Prednisolone Sodium Phosphate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisolone Sodium Phosphate NDC 0121-0773
- Generic Name
- Prednisolone Sodium Phosphate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisolone Sodium Phosphate NDC 0121-0777
- Generic Name
- Prednisolone Sodium Phosphate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPrednisolone NDC 0121-0885
- Generic Name
- Prednisolone
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0121-0904
- Generic Name
- Morphine Sulfate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Otc DrugLidocaine Pain Relief NDC 0121-0970
- Generic Name
- Lidocaine Pain Relief
- Dosage Form
- Patch
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-1047
- Generic Name
- Acetaminophen
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugPrednisolone Sodium Phosphate NDC 0121-1100
- Generic Name
- Prednisolone Sodium Phosphate
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugHydrocodone Bitartrate And Acetaminophen NDC 0121-1544
- Generic Name
- Hydrocodone Bitartrate And Acetaminophen
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-2094
- Generic Name
- Acetaminophen
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugHydrocodone Bitartrate And Acetaminophen NDC 0121-2316
- Generic Name
- Hydrocodone Bitartrate And Acetaminophen
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAcetaminophen NDC 0121-3141
- Generic Name
- Acetaminophen
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugHydrocodone Bitartrate And Acetaminophen NDC 0121-4772
- Generic Name
- Hydrocodone Bitartrate And Acetaminophen
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Parke-Davis Div of Pfizer Inc
NDC Product
Human Prescription DrugNardil NDC 0071-0350
- Generic Name
- Phenelzine Sulfate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Person and Covey
NDC Product
Human Otc DrugSolbar Shield Spf40 NDC 0096-0682
- Generic Name
- Solbar Shield Spf40
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSolbar Avo Spf35 NDC 0096-0687
- Generic Name
- Solbar Avo Spf35
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSolbar Sunscreen 35 Avo NDC 0096-0690
- Generic Name
- Sunscreen
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSolbar Sunscreen 40 Zinc NDC 0096-0691
- Generic Name
- Sunscreen
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugSolbar Sunscreen 40 Shield NDC 0096-0692
- Generic Name
- Sunscreen
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugDhs Sal NDC 0096-0812
- Generic Name
- Salicylic Acid
- Dosage Form
- Shampoo
- Route
- Topical
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Pfizer Laboratories Div Pfizer Inc
NDC Product
Human Prescription DrugAbrilada NDC 0025-0325
- Generic Name
- Adalimumab-afzb
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugAbrilada NDC 0025-0328
- Generic Name
- Adalimumab-afzb
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugAbrilada NDC 0025-0333
- Generic Name
- Adalimumab-afzb
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugPropofol NDC 0069-0209
- Generic Name
- Propofol
- Dosage Form
- Injection, Emulsion
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPropofol NDC 0069-0234
- Generic Name
- Propofol
- Dosage Form
- Injection, Emulsion
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRuxience NDC 0069-0238
- Generic Name
- Rituximab-pvvr
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugPropofol NDC 0069-0248
- Generic Name
- Propofol
- Dosage Form
- Injection, Emulsion
- Route
- Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRuxience NDC 0069-0249
- Generic Name
- Rituximab-pvvr
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugZirabev NDC 0069-0315
- Generic Name
- Bevacizumab-bvzr
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugZirabev NDC 0069-0342
- Generic Name
- Bevacizumab-bvzr
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugHympavzi NDC 0069-2151
- Generic Name
- Marstacimab-hncq
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugElrexfio NDC 0069-2522
- Generic Name
- Elranatamab-bcmm
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
NDC Product
Human Prescription DrugElrexfio NDC 0069-4494
- Generic Name
- Elranatamab-bcmm
- Dosage Form
- Injection, Solution
- Route
- Subcutaneous
- Marketing
- BLA
Active Listing
Pharmaceutical Associates, Inc.
NDC Product
Human Prescription DrugPropranolol Hydrochloride NDC 0121-0908
- Generic Name
- Propranolol Hydrochloride
- Dosage Form
- Solution
- Route
- Oral
- Marketing
- ANDA
Active Listing
Pharmacia & Upjohn Company LLC
NDC Product
Human Prescription DrugNicotrol NDC 0009-5401
- Generic Name
- Nicotine
- Dosage Form
- Spray, Metered
- Route
- Nasal
- Marketing
- NDA
Active Listing
Teva Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugDiclofenac Epolamine NDC 0093-3727
- Generic Name
- Diclofenac Epolamine
- Dosage Form
- System
- Route
- Topical
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugLiothyronine Sodium NDC 0093-2178
- Generic Name
- Liothyronine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLiothyronine Sodium NDC 0093-2179
- Generic Name
- Liothyronine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLiothyronine Sodium NDC 0093-2180
- Generic Name
- Liothyronine Sodium
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugEstradiol NDC 0093-3541
- Generic Name
- Estradiol
- Dosage Form
- Cream
- Route
- Vaginal
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevalbuterol NDC 0093-4145
- Generic Name
- Levalbuterol
- Dosage Form
- Solution
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevalbuterol NDC 0093-4146
- Generic Name
- Levalbuterol
- Dosage Form
- Solution
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLevalbuterol NDC 0093-4148
- Generic Name
- Levalbuterol
- Dosage Form
- Solution
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBudesonide NDC 0093-6815
- Generic Name
- Budesonide
- Dosage Form
- Suspension
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBudesonide NDC 0093-6815
- Generic Name
- Budesonide
- Dosage Form
- Suspension
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBudesonide NDC 0093-6816
- Generic Name
- Budesonide
- Dosage Form
- Suspension
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBudesonide NDC 0093-6816
- Generic Name
- Budesonide
- Dosage Form
- Suspension
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBudesonide NDC 0093-6817
- Generic Name
- Budesonide
- Dosage Form
- Suspension
- Route
- Respiratory (inhalation)
- Marketing
- ANDA
Active Listing
Viatris Specialty LLC
NDC Product
Human Prescription DrugDymista NDC 0037-0245
- Generic Name
- Azelastine Hydrochloride And Fluticasone Propionate
- Dosage Form
- Spray, Metered
- Route
- Nasal
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugElestrin NDC 0037-4801
- Generic Name
- Estradiol
- Dosage Form
- Gel, Metered
- Route
- Topical
- Marketing
- NDA
Active Listing
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
NDC Product
Human Prescription DrugProtonix I.v. NDC 0008-0923
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugProtonix I.v. NDC 0008-4001
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intravenous
- Marketing
- NDA
Active Listing
Xttrium Laboratories, Inc
NDC Product
Human Prescription Drug- Generic Name
- Promethazine Hydrochloride And Dextromethorphan Hydrobromide
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- ANDA
Active Listing
Xttrium Laboratories, Inc.
NDC Product
Human Prescription DrugPromethazine Hydrochloride NDC 0116-4023
- Generic Name
- Promethazine Hydrochloride
- Dosage Form
- Syrup
- Route
- Oral
- Marketing
- ANDA
Active Listing
sanofi-aventis U.S. LLC
NDC Product
Human Prescription DrugPriftin NDC 0088-2102
- Generic Name
- Rifapentine
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
