HYPROMELLOSE 2208 (100 MPA.S)
UNII B1QE5P712K

Substance Identification & Data

This profile provides standardized clinical and technical data for Hypromellose 2208 (100 Mpa.s), uniquely identified by the FDA Unique Ingredient Identifier (UNII) B1QE5P712K.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9004-65-3 and the RxNorm Concept ID (RxCUI) 1300444. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
B1QE5P712K
CAS Registry Number
9004-65-3
RxNorm Concept ID
1300444

Detailed Substance Profile

Preferred Name
HYPROMELLOSE 2208 (100 MPA.S)
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
B1QE5P712K
The specific atomic composition represented as a molecular structure string.
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 Hypromellose 2208 (100 Mpa.s). 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

HPMC 2208 (100 CPS)
HYDROXYPROPYL METHYLCELLULOSE 100
HYDROXYPROPYL METHYLCELLULOSE 100 [II]
HYDROXYPROPYL METHYLCELLULOSE 2208 (100 CPS)
HYDROXYPROPYLMETHYLCELLULOSE 2208, 100 CPS
HYPROMELLOSE 2208 (100 CPS)
HYPROMELLOSE 2208 (100 MPA.S)

Brand / Trade Names

BENECEL HPMC K100
HYPROMELLOSE 90SH-100SR
METHOCEL K100
METHOCEL K100 PREMIUM LV
METHOCEL K100LV
METHOCEL K100-LV
METHOCEL K-100LV
METHOCEL K-100-LV
METOLOSE 90SH 100SR

NDC Products Containing HYPROMELLOSE 2208 (100 MPA.S)

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.
→ A-S Medication Solutions 11
→ AMERISOURCE BERGEN 1
→ ANI Pharmaceuticals, Inc. 1
→ Accord Healthcare Inc. 2
→ Accord Healthcare, Inc. 3
→ Acella Pharmaceuticals, LLC 1
→ Acme United Corporation 1
→ Actavis Pharma, Inc. 4
→ Ajanta Pharma USA Inc. 3
→ American Health Packaging 3
→ Amneal Pharmaceuticals NY LLC 2
→ Aphena Pharma Solutions - Tennessee, LLC 4
→ Apotex Corp. 5
→ Aurobindo Pharma Limited 5
→ AvKARE 4
→ AvPAK 3
→ BETTER LIVING BRANDS LLC. 1
→ BPI Labs LLC 1
→ Bausch & Lomb Incorporated 1
→ CVS 1
→ CVS Pharamacy, Inc 1
→ Camber Pharmaceuticals, Inc. 6
→ Carlsbad Technology, Inc. 3
→ Chartwell RX, LLC 5
→ Cranbury Pharmaceuticals, LLC 4
→ Dr. Reddys Laboratories Limited 1
→ Dr.Reddys Laboratories, Inc. 1
→ Edenbridge Pharmaceuticals LLC. 2
→ Efficient Laboratories Inc 2
→ Endo USA, Inc. 1
→ Epic Pharma LLC 2
→ Epic Pharma, LLC 6
→ Golden State Medical Supply, Inc. 6
→ Granules India Limited 4
→ Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. 1
→ Hikma Pharmaceuticals USA Inc. 5
→ INNOVUS PHARMACEUTICALS, INC. 2
→ KRAMER LABORATORIES 2
→ Lannett Company, Inc. 9
→ Llorens Pharmaceuticals International Division 1
→ Lupin Pharmaceuticals,Inc. 6
→ MARKSANS PHARMA LIMITED 2
→ Medsource Pharmaceuticals 1
→ Menper Distributors, Inc. 1
→ Micro Labs Limited 2
→ NorthStar Rx LLC 2
→ Northwind Health Company, LLC 2
→ Ohm Laboratories Inc. 1
→ PD-Rx Pharmaceuticals, Inc. 5
→ Par Health USA, LLC 5
→ Proficient Rx LP 3
→ PuraCap Laboratories LLC 2
→ PuraCap Pharmaceutical LLC 1
→ Rising Pharma Holdings, Inc. 4
→ Rite Aid 1
→ Rugby Laboratories 1
→ Safeway, Inc. 1
→ Sandoz Inc 1
→ Sandoz Inc. 3
→ Shandong New Time Pharmaceutical Co., Ltd. 1
→ Solco Healthcare U.S., LLC 4
→ St. Mary�s Medical Park Pharmacy 1
→ Sun Pharmaceutical Industries, Inc. 3
→ THE KROGER COMPANY 1
→ TIME CAP LABORATORIES, INC 2
→ TWIN MED, LLC 1
→ Target Corporation. 1
→ Tec Laboratories Inc. 2
→ Teva Pharmaceuticals USA, Inc. 2
→ Teva Pharmaceuticals, Inc. 2
→ Torrent Pharmaceuticals Limited 2
→ Trigen Laboratories, LLC 4
→ UP & UP 1
→ Unichem Pharmaceuticals (USA), Inc. 5
→ WALGREEN CO. 1
→ WALGREENS CO. 1
→ Walgreen Company 1

A-S Medication Solutions

NDC Product
Human Prescription Drug

Etodolac
NDC 50090-1790

Generic Name
Etodolac
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 50090-4737

Generic Name
Divalproex Sodium
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Desvenlafaxine
NDC 50090-4806

Generic Name
Desvenlafaxine
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tacrolimus
NDC 50090-5596

Generic Name
Tacrolimus
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Felodipine
NDC 50090-5870

Generic Name
Felodipine
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 50090-6074

Generic Name
Divalproex Sodium
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Metformin
NDC 50090-7372

Generic Name
Metformin Er 750 Mg
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Metformin
NDC 50090-7373

Generic Name
Metformin Er 750 Mg
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Alprazolam
NDC 50090-7556

Generic Name
Alprazolam
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium
NDC 50090-7646

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium
NDC 50090-7647

Generic Name
Diclofenac Sodium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

AMERISOURCE BERGEN

NDC Product
Human Otc Drug

Omeprazole
NDC 46122-686

Generic Name
Omeprazole
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

ANI Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Tranexamic Acid
NDC 62559-265

Generic Name
Tranexamic Acid
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Accord Healthcare Inc.

NDC Product
Human Prescription Drug

Quetiapine Fumarate
NDC 16729-132

Generic Name
Quetiapine Fumarate
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Dalfampridine
NDC 16729-292

Generic Name
Dalfampridine
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Accord Healthcare, Inc.

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 16729-303

Generic Name
Diltiazem Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 16729-304

Generic Name
Diltiazem Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 16729-305

Generic Name
Diltiazem Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Acella Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Nicotinamide
NDC 42192-374

Generic Name
Nicotinamide
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Acme United Corporation

NDC Product
Human Otc Drug

Physicianscare Allergy Antihistamine
NDC 0924-0056

Generic Name
Diphenhydramine Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Actavis Pharma, Inc.

NDC Product
Human Prescription Drug

Methylphenidate Hydrochloride
NDC 62037-725

Generic Name
Methylphenidate Hydrochloride
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Methylphenidate Hydrochloride
NDC 62037-726

Generic Name
Methylphenidate Hydrochloride
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Methylphenidate Hydrochloride
NDC 62037-727

Generic Name
Methylphenidate Hydrochloride
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Methylphenidate Hydrochloride
NDC 62037-734

Generic Name
Methylphenidate Hydrochloride
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Ajanta Pharma USA Inc.

NDC Product
Human Prescription Drug

Oxybutynin Chloride
NDC 27241-155

Generic Name
Oxybutynin Chloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxybutynin Chloride
NDC 27241-156

Generic Name
Oxybutynin Chloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxybutynin Chloride
NDC 27241-157

Generic Name
Oxybutynin Chloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

American Health Packaging

NDC Product
Human Prescription Drug

Phenytoin
NDC 60687-156

Generic Name
Phenytoin
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Desvenlafaxine
NDC 60687-607

Generic Name
Desvenlafaxine
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tranexamic Acid
NDC 60687-750

Generic Name
Tranexamic Acid
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Amneal Pharmaceuticals NY LLC

NDC Product
Human Prescription Drug

Theophylline
NDC 60219-2045

Generic Name
Theophylline
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Theophylline
NDC 60219-2046

Generic Name
Theophylline
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Aphena Pharma Solutions - Tennessee, LLC

NDC Product
Human Prescription Drug

Oxybutynin Chloride Extended Release
NDC 43353-282

Generic Name
Oxybutynin Chloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxybutynin Chloride Extended Release
NDC 43353-284

Generic Name
Oxybutynin Chloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxybutynin Chloride Extended Release
NDC 43353-285

Generic Name
Oxybutynin Chloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxybutynin Chloride Extended Release
NDC 43353-322

Generic Name
Oxybutynin Chloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Apotex Corp.

NDC Product
Human Prescription Drug

Etodolac
NDC 60505-0041

Generic Name
Etodolac
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Etodolac
NDC 60505-0102

Generic Name
Etodolac
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxcarbazepine
NDC 60505-4128

Generic Name
Oxcarbazepine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxcarbazepine
NDC 60505-4129

Generic Name
Oxcarbazepine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxcarbazepine
NDC 60505-4130

Generic Name
Oxcarbazepine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Aurobindo Pharma Limited

NDC Product
Human Prescription Drug

Nifedipine
NDC 59651-295

Generic Name
Nifedipine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nifedipine
NDC 59651-296

Generic Name
Nifedipine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nifedipine
NDC 59651-297

Generic Name
Nifedipine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Mesalamine
NDC 59651-397

Generic Name
Mesalamine
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Estradiol Vaginal Inserts
NDC 59651-439

Generic Name
Estradiol
Dosage Form
Tablet, Film Coated
Route
Vaginal
Marketing
ANDA
Active Listing

AvKARE

NDC Product
Human Prescription Drug

Oxybutynin Chloride Extended Release
NDC 42291-633

Generic Name
Oxybutynin Chloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxybutynin Chloride Extended Release
NDC 42291-634

Generic Name
Oxybutynin Chloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxybutynin Chloride Extended Release
NDC 42291-635

Generic Name
Oxybutynin Chloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Theophylline
NDC 42291-922

Generic Name
Theophylline
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

AvPAK

NDC Product
Human Prescription Drug

Oxybutynin Chloride Extended Release
NDC 50268-627

Generic Name
Oxybutynin Chloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxybutynin Chloride Extended Release
NDC 50268-628

Generic Name
Oxybutynin Chloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxybutynin Chloride Extended Release
NDC 50268-629

Generic Name
Oxybutynin Chloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

BETTER LIVING BRANDS LLC.

NDC Product
Human Otc Drug

Acetaminophen Diphenhydramine Hcl
NDC 21130-354

Generic Name
Acetaminophen Diphenhydramine Hcl
Dosage Form
Tablet
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

BPI Labs LLC

NDC Product
Human Prescription Drug

Tacrolimus
NDC 54288-135

Generic Name
Tacrolimus
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

Bausch & Lomb Incorporated

NDC Product
Human Otc Drug

Muro 128
NDC 24208-277

Generic Name
Sodium Chloride
Dosage Form
Solution
Route
Ophthalmic
Marketing
OTC MONOGRAPH DRUG
Active Listing

CVS

NDC Product
Human Otc Drug

Esomeprazole
NDC 51316-715

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

CVS Pharamacy, Inc

NDC Product
Human Otc Drug

Omeprazole
NDC 51316-061

Generic Name
Omeprazole
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Camber Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Fesoterodine Fumarate
NDC 31722-033

Generic Name
Fesoterodine Fumarate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Fesoterodine Fumarate
NDC 31722-034

Generic Name
Fesoterodine Fumarate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Mesalamine
NDC 31722-043

Generic Name
Mesalamine
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Theophylline
NDC 31722-077

Generic Name
Theophylline
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Theophylline
NDC 31722-078

Generic Name
Theophylline
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Mesalamine
NDC 31722-489

Generic Name
Mesalamine
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Carlsbad Technology, Inc.

NDC Product
Human Prescription Drug

Felodipine
NDC 61442-431

Generic Name
Felodipine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Felodipine
NDC 61442-432

Generic Name
Felodipine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Felodipine
NDC 61442-433

Generic Name
Felodipine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Chartwell RX, LLC

NDC Product
Human Prescription Drug

Paroxetine
NDC 62135-425

Generic Name
Paroxetine
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Paroxetine
NDC 62135-426

Generic Name
Paroxetine
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Paroxetine
NDC 62135-427

Generic Name
Paroxetine
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Theophylline
NDC 62135-457

Generic Name
Theophylline
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Isosorbide Mononitrate
NDC 62135-588

Generic Name
Isosorbide Mononitrate
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Cranbury Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Rosuvastatin Calcium
NDC 27808-155

Generic Name
Rosuvastatin Calcium
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rosuvastatin Calcium
NDC 27808-156

Generic Name
Rosuvastatin Calcium
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rosuvastatin Calcium
NDC 27808-157

Generic Name
Rosuvastatin Calcium
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rosuvastatin Calcium
NDC 27808-158

Generic Name
Rosuvastatin Calcium
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Dr. Reddys Laboratories Limited

NDC Product
Human Prescription Drug

Donepezil Hydrochloride
NDC 55111-302

Generic Name
Donepezil Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Dr.Reddys Laboratories, Inc.

NDC Product
Human Prescription Drug

Colchicine
NDC 43598-372

Generic Name
Colchicine
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Edenbridge Pharmaceuticals LLC.

NDC Product
Human Prescription Drug

Donepezil Hydrochloride
NDC 42799-954

Generic Name
Donepezil Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Isosorbide Mononitrate
NDC 42799-960

Generic Name
Isosorbide Mononitrate
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Efficient Laboratories Inc

NDC Product
Human Otc Drug

Hongo Killer
NDC 58593-601

Generic Name
Undecylenic Acid
Dosage Form
Spray
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Hongo Killer
NDC 58593-826

Generic Name
Undecylenic Acid
Dosage Form
Liquid
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Endo USA, Inc.

NDC Product
Human Prescription Drug

Praziquantel
NDC 49884-231

Generic Name
Praziquantel
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Epic Pharma LLC

NDC Product
Human Prescription Drug

Betaxolol
NDC 42806-038

Generic Name
Betaxolol
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Betaxolol
NDC 42806-039

Generic Name
Betaxolol
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Epic Pharma, LLC

NDC Product
Human Prescription Drug

Citalopram
NDC 42806-019

Generic Name
Citalopram
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Citalopram
NDC 42806-020

Generic Name
Citalopram
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Citalopram
NDC 42806-021

Generic Name
Citalopram
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Trandolapril
NDC 42806-052

Generic Name
Trandolapril Tablets
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Trandolapril
NDC 42806-053

Generic Name
Trandolapril Tablets
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Trandolapril
NDC 42806-054

Generic Name
Trandolapril Tablets
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Golden State Medical Supply, Inc.

NDC Product
Human Prescription Drug

Felodipine
NDC 51407-088

Generic Name
Felodipine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Felodipine
NDC 51407-089

Generic Name
Felodipine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Zileuton
NDC 51407-741

Generic Name
Zileuton
Dosage Form
Tablet, Multilayer, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Erythromycin
NDC 51407-853

Generic Name
Erythromycin
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Erythromycin
NDC 51407-854

Generic Name
Erythromycin
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Citalopram
NDC 60429-175

Generic Name
Citalopram
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Granules India Limited

NDC Product
Human Otc Drug

Ibuprofen
NDC 62207-365

Generic Name
Ibuprofen
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 62207-365

Generic Name
Ibuprofen
Dosage Form
Tablet
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing

NDC 62207-366

Generic Name
Ibuprofen
Dosage Form
Tablet
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Otc Drug

Ibuprofen
NDC 62207-366

Generic Name
Ibuprofen
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Theophylline
NDC 23155-742

Generic Name
Theophylline
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Hikma Pharmaceuticals USA Inc.

NDC Product
Human Prescription Drug

Desvenlafaxine
NDC 0054-0400

Generic Name
Desvenlafaxine
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Desvenlafaxine
NDC 0054-0401

Generic Name
Desvenlafaxine
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rufinamide
NDC 0054-0425

Generic Name
Rufinamide
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rufinamide
NDC 0054-0426

Generic Name
Rufinamide
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Desvenlafaxine
NDC 0054-0603

Generic Name
Desvenlafaxine
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

INNOVUS PHARMACEUTICALS, INC.

NDC Product
Human Otc Drug

Omeprazole
NDC 57483-740

Generic Name
Omeprazole
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Esomeprazole
NDC 57483-900

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

KRAMER LABORATORIES

Lannett Company, Inc.

NDC Product
Human Prescription Drug

Fluvastatin Sodium
NDC 0527-2580

Generic Name
Fluvastatin Sodium
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxybutynin Chloride Extended Release
NDC 62175-270

Generic Name
Oxybutynin Chloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxybutynin Chloride Extended Release
NDC 62175-271

Generic Name
Oxybutynin Chloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxybutynin Chloride Extended Release
NDC 62175-272

Generic Name
Oxybutynin Chloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Paroxetine Hydrochloride
NDC 62175-470

Generic Name
Paroxetine Hydrochloride
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Paroxetine Hydrochloride
NDC 62175-471

Generic Name
Paroxetine Hydrochloride
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Paroxetine Hydrochloride
NDC 62175-472

Generic Name
Paroxetine Hydrochloride
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Esomeprazole Magnesium
NDC 62175-820

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release Pellets
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Esomeprazole Magnesium
NDC 62175-840

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release Pellets
Route
Oral
Marketing
ANDA
Active Listing

Llorens Pharmaceuticals International Division

NDC Product
Human Otc Drug

Dermagesic
NDC 54859-120

Generic Name
Pramoxine Hcl, Zinc Oxide, Calamine
Dosage Form
Liquid
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Lupin Pharmaceuticals,Inc.

NDC Product
Human Prescription Drug

Linezolid
NDC 43386-022

Generic Name
Linezolid
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate
NDC 43386-540

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate
NDC 43386-541

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate
NDC 43386-542

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate
NDC 43386-543

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate
NDC 43386-544

Generic Name
Morphine Sulfate
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

MARKSANS PHARMA LIMITED

NDC Product
Human Prescription Drug

Metformin Hydrochloride
NDC 25000-101

Generic Name
Metformin Hydrochloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Metformin Hydrochloride
NDC 25000-102

Generic Name
Metformin Hydrochloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Medsource Pharmaceuticals

NDC Product
Human Prescription Drug

Etodolac
NDC 45865-206

Generic Name
Etodolac
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Menper Distributors, Inc.

NDC Product
Human Otc Drug

Defensol D
NDC 53145-005

Generic Name
Acetaminophen, Chlorpherinamine Maleate, Phenylephrine Hci
Dosage Form
Tablet
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Micro Labs Limited

NDC Product
Human Prescription Drug

Rufinamide
NDC 42571-391

Generic Name
Rufinamide
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rufinamide
NDC 42571-392

Generic Name
Rufinamide
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

NorthStar Rx LLC

NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 16714-484

Generic Name
Divalproex Sodium
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 16714-485

Generic Name
Divalproex Sodium
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Northwind Health Company, LLC

NDC Product
Human Prescription Drug

Alfuzosin Hydrochloride
NDC 51655-087

Generic Name
Alfuzosin Hydrochloride
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Ohm Laboratories Inc.

NDC Product
Human Otc Drug

Esomeprazole
NDC 51660-027

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

PD-Rx Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Etodolac
NDC 43063-578

Generic Name
Etodolac
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Etodolac
NDC 43063-671

Generic Name
Etodolac
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Oxybutynin Chloride Extended Release
NDC 43063-790

Generic Name
Oxybutynin Chloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Etodolac
NDC 43063-856

Generic Name
Etodolac
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Par Health USA, LLC

Proficient Rx LP

NDC Product
Human Prescription Drug

Alprazolam
NDC 63187-445

Generic Name
Alprazolam
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Alprazolam
NDC 63187-518

Generic Name
Alprazolam
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Etodolac
NDC 63187-736

Generic Name
Etodolac
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

PuraCap Laboratories LLC

NDC Product
Human Prescription Drug

Betaxolol
NDC 24658-700

Generic Name
Betaxolol
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Betaxolol
NDC 24658-701

Generic Name
Betaxolol
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

PuraCap Pharmaceutical LLC

NDC Product
Human Otc Drug

Ibuprofen
NDC 51013-319

Generic Name
Ibuprofen
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Rising Pharma Holdings, Inc.

NDC Product
Human Prescription Drug

Felodipine
NDC 57237-108

Generic Name
Felodipine
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Felodipine
NDC 57237-109

Generic Name
Felodipine
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Felodipine
NDC 57237-110

Generic Name
Felodipine
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Alfuzosin Hydrochloride
NDC 57237-114

Generic Name
Alfuzosin Hydrochloride
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Rite Aid

NDC Product
Human Otc Drug

Omeprazole
NDC 11822-0061

Generic Name
Omeprazole
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Rugby Laboratories

Safeway, Inc.

NDC Product
Human Otc Drug

Esomeprazole
NDC 21130-926

Generic Name
Esomeprazole
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Sandoz Inc

NDC Product
Human Prescription Drug

Omeprazole
NDC 0781-2234

Generic Name
Omeprazole
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Sandoz Inc.

NDC Product
Human Prescription Drug

Tacrolimus
NDC 0781-2102

Generic Name
Tacrolimus
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tacrolimus
NDC 0781-2103

Generic Name
Tacrolimus
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tacrolimus
NDC 0781-2104

Generic Name
Tacrolimus
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

Shandong New Time Pharmaceutical Co., Ltd.

NDC Product
Human Prescription Drug

Isosorbide Mononitrate
NDC 42677-307

Generic Name
Isosorbide Mononitrate
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Solco Healthcare U.S., LLC

NDC Product
Human Prescription Drug

Quetiapine
NDC 43547-019

Generic Name
Quetiapine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Quetiapine
NDC 43547-020

Generic Name
Quetiapine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Quetiapine
NDC 43547-021

Generic Name
Quetiapine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Quetiapine
NDC 43547-022

Generic Name
Quetiapine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

St. Mary�s Medical Park Pharmacy

NDC Product
Human Prescription Drug

Etodolac
NDC 60760-552

Generic Name
Etodolac
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Sun Pharmaceutical Industries, Inc.

NDC Product
Human Prescription Drug

Ranolazine
NDC 63304-017

Generic Name
Ranolazine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Ranolazine
NDC 63304-018

Generic Name
Ranolazine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Erlotinib
NDC 63304-095

Generic Name
Erlotinib
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

THE KROGER COMPANY

NDC Product
Human Otc Drug

Esomeprazole
NDC 30142-989

Generic Name
Esomeprazole
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

TIME CAP LABORATORIES, INC

TWIN MED, LLC

NDC Product
Human Otc Drug

Cetirizine Hydrochloride 10 Mg
NDC 55681-302

Generic Name
Cetirizine Hydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Target Corporation.

NDC Product
Human Otc Drug

Up And Up Fiber Therapy
NDC 11673-620

Generic Name
Calcium Polycarbophil
Dosage Form
Tablet
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Tec Laboratories Inc.

NDC Product
Human Otc Drug

Tecnu Ivy Complete Kit
NDC 51879-400

Generic Name
Ivy Treatment
Dosage Form
Kit
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Tecnu Calagel
NDC 51879-802

Generic Name
Diphenhydramine Hydrochloride
Dosage Form
Gel
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Teva Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Cefaclor
NDC 0093-1087

Generic Name
Cefaclor
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Estradiol
NDC 0093-3223

Generic Name
Estradiol
Dosage Form
Insert
Route
Vaginal
Marketing
ANDA
Active Listing

Teva Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Theophylline
NDC 0480-3309

Generic Name
Theophylline
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Theophylline
NDC 0480-3310

Generic Name
Theophylline
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Torrent Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Erythromycin
NDC 13668-586

Generic Name
Erythromycin
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Erythromycin
NDC 13668-588

Generic Name
Erythromycin
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Trigen Laboratories, LLC

NDC Product
Human Prescription Drug

Hydromorphone Hydrochloride
NDC 13811-701

Generic Name
Hydromorphone Hydrochloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Hydromorphone Hydrochloride
NDC 13811-702

Generic Name
Hydromorphone Hydrochloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Hydromorphone Hydrochloride
NDC 13811-703

Generic Name
Hydromorphone Hydrochloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Hydromorphone Hydrochloride
NDC 13811-704

Generic Name
Hydromorphone Hydrochloride
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

UP & UP

NDC Product
Human Otc Drug

Omeprazole
NDC 11673-948

Generic Name
Omeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Unichem Pharmaceuticals (USA), Inc.

NDC Product
Human Prescription Drug

Quetiapine
NDC 29300-308

Generic Name
Quetiapine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Quetiapine
NDC 29300-309

Generic Name
Quetiapine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Quetiapine
NDC 29300-310

Generic Name
Quetiapine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Quetiapine
NDC 29300-311

Generic Name
Quetiapine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Quetiapine
NDC 29300-312

Generic Name
Quetiapine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

WALGREEN CO.

NDC Product
Human Otc Drug

Acetaminophen
NDC 0363-9798

Generic Name
Acetaminophen
Dosage Form
Tablet
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

WALGREENS CO.

NDC Product
Human Otc Drug

Acetaminophen Diphenhydramine Hcl
NDC 0363-9664

Generic Name
Acetaminophen Diphenhydramine Hcl
Dosage Form
Tablet
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Walgreen Company

NDC Product
Human Otc Drug

Omeprazole
NDC 0363-9980

Generic Name
Omeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

External Clinical & Regulatory Resources

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