NDC Product
Human Otc DrugAcid Reducer NDC 10202-722
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Substance Identification & Data
This profile provides standardized clinical and technical data for Methacrylic Acid And Ethyl Acrylate Copolymer, uniquely identified by the FDA Unique Ingredient Identifier (UNII) NX76LV5T8J.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 25212-88-8 and the RxNorm Concept ID (RxCUI) 1309718. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
NX76LV5T8J
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
Substance Type
polymer
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for Methacrylic Acid And Ethyl Acrylate Copolymer. 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
METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER
OF
Common Names & Synonyms
ETHYL ACRYLATE AND METHACRYLIC ACID COPOLYMER (1:1; 250000 MW)
CN
ETHYL ACRYLATE-METHACRYLIC ACID COPOLYMER
CN
ETHYL ACRYLATE-METHACRYLIC ACID COPOLYMER [II]
CN
EUDRAGIT L 100-55 [II]
CN
EUDRAGIT L 30 D
CN
EUDRAGIT L 30 D [II]
CN
METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER [USP IMPURITY]
CN
METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER [USP-RS]
CN
METHACRYLIC ACID COPOLYMER TYPE C
CN
METHACRYLIC ACID COPOLYMER TYPE C [II]
CN
METHACRYLIC ACID-ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
CN
METHACRYLIC ACID-ETHYL ACRYLATE COPOLYMER (1:1) TYPE A [II]
CN
METHACRYLIC ACID-ETHYL ACRYLATE COPOLYMER (1:1) TYPE A 30% DISPERSION
CN
Brand / Trade Names
EUDRAGIT L 100-55
BN
EUDRAGIT L 30 D-55
BN
EUDRAGIT L30 D-55
BN
KOLLICOAT MAE 100 P
BN
KOLLICOAT MAE 30 DP
BN
NDC Products Containing METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER
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
7-Eleven
Active Listing
Actavis Pharma, Inc.
NDC Product
Human Prescription DrugAlprazolam NDC 0228-4019
- Generic Name
- Alprazolam
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAlprazolam NDC 0228-4022
- Generic Name
- Alprazolam
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAlprazolam NDC 0228-4024
- Generic Name
- Alprazolam
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAlprazolam NDC 0228-4025
- Generic Name
- Alprazolam
- Dosage Form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiclofenac Sodium And Misoprostol NDC 0591-0397
- Generic Name
- Diclofenac Sodium And Misoprostol
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiclofenac Sodium And Misoprostol NDC 0591-0398
- Generic Name
- Diclofenac Sodium And Misoprostol
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDoxylamine Succinate And Pyridoxine Hydrochloride NDC 0591-2132
- Generic Name
- Doxylamine Succinate And Pyridoxine Hydrochloride
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Xl NDC 0591-3331
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0591-3854
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0591-3862
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0591-3869
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0591-3873
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0591-3891
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0591-3895
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMethylphenidate Hydrochloride NDC 0591-3902
- Generic Name
- Methylphenidate Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
AiPing Pharmaceutical, Inc.
NDC Product
Human Prescription DrugDoxycycline NDC 11788-134
- Generic Name
- Doxycycline
- Dosage Form
- Capsule
- 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
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 DrugMorphine Sulfate NDC 0115-1277
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1278
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1279
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1280
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1281
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1282
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0115-1479
- Generic Name
- Morphine Sulfate
- 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
NDC Product
Human Prescription DrugTamsulosin Hydrochloride NDC 0115-8211
- Generic Name
- Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
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
Galderma Laboratories, L.P.
NDC Product
Human Prescription DrugOracea NDC 0299-3822
- Generic Name
- Doxycycline
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
KVK-Tech, Inc.
NDC Product
Human Otc DrugChlorphen-12 NDC 10702-017
- Generic Name
- Chlorpheniramine Maleate
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
L. Perrigo Company
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 0113-2022
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Lannett Company Inc.
NDC Product
Human Prescription DrugBupropion Hydrochloride (xl) NDC 0527-2415
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride (xl) NDC 0527-2430
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended 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
Major Pharmaceuticals
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 0904-6474
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOxybutynin Chloride NDC 0904-6570
- Generic Name
- Oxybutynin Chloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLansoprazole NDC 0904-6662
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMycophenolic Acid NDC 0904-6785
- Generic Name
- Mycophenolic Acid
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 0904-6860
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 0904-6861
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 0904-6870
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPosaconazole NDC 0904-7149
- Generic Name
- Posaconazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugAcamprosate Calcium NDC 0904-7213
- Generic Name
- Acamprosate Calcium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDabigatran Etexilate NDC 0904-7253
- Generic Name
- Dabigatran Etexilate
- Dosage Form
- Capsule, Coated Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDabigatran Etexilate NDC 0904-7254
- Generic Name
- Dabigatran Etexilate
- Dosage Form
- Capsule, Coated Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDabigatran Etexilate NDC 0904-7255
- Generic Name
- Dabigatran Etexilate
- Dosage Form
- Capsule, Coated Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBudesonide NDC 0904-7313
- Generic Name
- Budesonide
- Dosage Form
- Capsule, Coated Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTamsulosin Hydrochloride NDC 0904-7383
- Generic Name
- Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride Xl NDC 0904-7469
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRanolazine NDC 0904-7506
- Generic Name
- Ranolazine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Mylan Pharmaceuticals Inc.
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 DrugVerapamil Hydrochloride NDC 0378-6320
- Generic Name
- Verapamil Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVerapamil Hydrochloride NDC 0378-6380
- Generic Name
- Verapamil Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugVerapamil Hydrochloride NDC 0378-6440
- Generic Name
- Verapamil Hydrochloride
- Dosage Form
- Capsule, 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 DrugLansoprazole NDC 0378-8015
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLansoprazole NDC 0378-8030
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release Pellets
- Route
- Oral
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 0615-7629
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugTamsulosin Hydrochloride NDC 0615-8055
- Generic Name
- Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 0615-8113
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 0615-8379
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 0615-8380
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDiltiazem Hydrochloride NDC 0615-8381
- Generic Name
- Diltiazem Hydrochloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 0615-8406
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 0615-8504
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBupropion Hydrochloride NDC 0615-8505
- Generic Name
- Bupropion Hydrochloride
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 0615-8586
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 0615-8587
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugDivalproex Sodium NDC 0615-8588
- Generic Name
- Divalproex Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugRanolazine NDC 0615-8611
- Generic Name
- Ranolazine
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugAdult Low Dose Aspirin NDC 0615-8613
- Generic Name
- Aspirin
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription DrugEsomeprazole Magnesium NDC 0615-8628
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Padagis US LLC
NDC Product
Human Prescription DrugTrospium Chloride Er NDC 0574-0118
- Generic Name
- Trospium Chloride
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugBudesonide NDC 0574-9855
- Generic Name
- Budesonide
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- NDA
Active Listing
Par Health USA, LLC
NDC Product
Human Prescription DrugLamotrigine Extended-release NDC 10370-207
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLamotrigine Extended-release NDC 10370-208
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLamotrigine Extended-release NDC 10370-256
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugLamotrigine Extended-release NDC 10370-334
- Generic Name
- Lamotrigine
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Reese Pharmaceutical Co
NDC Product
Human Otc DrugPreferred Antibacterial Plus Urinary Pain Relief NDC 10956-763
- Generic Name
- Methenamine, Sodium Salicylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Rite Aid
NDC Product
Human Otc DrugOmeprazole NDC 11822-0061
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugRite Aid Antibacterial Plus Urinary Pain Relief NDC 11822-4892
- Generic Name
- Methenamine, Sodium Salicylate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
Rite Aid Corporation
NDC Product
Human Otc DrugLansoprazole NDC 11822-0019
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugEsomeprazole Magnesium NDC 11822-0024
- Generic Name
- Esomeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugSinus Relief Daytime, Nighttime NDC 11822-5694
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Guaifenesin, Phenylephri...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rugby Laboratories
NDC Product
Human Otc DrugAcid Reducer NDC 0536-1322
- Generic Name
- Omeprazole
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Rugby Laboratories, Inc
NDC Product
Human Otc DrugLansoprazole NDC 0536-1368
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Sandoz Inc
NDC Product
Human Prescription DrugTamsulosin Hydrochloride NDC 0781-2076
- Generic Name
- Tamsulosin Hydrochloride
- Dosage Form
- Capsule
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 0781-2785
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 0781-2790
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 0781-2859
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOmeprazole NDC 0781-2868
- Generic Name
- Omeprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClarithromycin NDC 0781-6022
- Generic Name
- Clarithromycin
- Dosage Form
- For Suspension
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugClarithromycin NDC 0781-6023
- Generic Name
- Clarithromycin
- Dosage Form
- For Suspension
- Route
- Oral
- Marketing
- ANDA
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
TARGET CORPORATION
NDC Product
Human Otc DrugAspirin NDC 11673-181
- Generic Name
- Aspirin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Target Corporation
NDC Product
Human Otc DrugDaytime Nighttime Sinus Relief NDC 11673-282
- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Guaifenesin, Phenylephri...
- Dosage Form
- Kit
- Route
- N/A
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugLansoprazole NDC 11673-324
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Otc DrugUp And Up Esomeprazole Magnesium NDC 11673-753
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed 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 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
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
Torrent Pharmaceuticals Limited
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 13668-096
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugPantoprazole Sodium NDC 13668-429
- Generic Name
- Pantoprazole Sodium
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription Drug- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Granule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugErythromycin NDC 13668-586
- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugErythromycin NDC 13668-588
- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugErythromycin NDC 13668-606
- Generic Name
- Erythromycin
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
UP & UP
NDC Product
Human Otc DrugOmeprazole NDC 11673-948
- Generic Name
- Omeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Upsher-Smith Laboratories, LLC
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0832-0225
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0832-0226
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0832-0227
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0832-0228
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0832-0229
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0832-0230
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, Extended Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMorphine Sulfate NDC 0832-0233
- Generic Name
- Morphine Sulfate
- Dosage Form
- Capsule, 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
Walgreen Company
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 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 Drug- Generic Name
- Acetaminophen, Diphenhydramine Hcl, Guaifenesin, Phenylephri...
- Dosage Form
- Kit
- Route
- N/A
- 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 DrugEsomeprazole Magnesium NDC 0363-3298
- Generic Name
- Esomeprazole Magnesium
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Marketing
- ANDA
Active Listing
Walgreens company
NDC Product
Human Otc DrugLansoprazole NDC 0363-0037
- Generic Name
- Lansoprazole
- Dosage Form
- Capsule, 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
