HYPROMELLOSE 2910 (3 MPA.S)
UNII 0VUT3PMY82

Substance Identification & Data

This profile provides standardized clinical and technical data for Hypromellose 2910 (3 Mpa.s), uniquely identified by the FDA Unique Ingredient Identifier (UNII) 0VUT3PMY82.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9004-65-3 and the RxNorm Concept ID (RxCUI) 1300449. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
0VUT3PMY82
CAS Registry Number
9004-65-3
RxNorm Concept ID
1300449

Detailed Substance Profile

Preferred Name
HYPROMELLOSE 2910 (3 MPA.S)
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
0VUT3PMY82
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
C82311
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 Hypromellose 2910 (3 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 603
HYDROXYPROPYL METHYLCELLULOSE 3CP
HYDROXYPROPYL METHYLCELLULOSE 603
HYDROXYPROPYL METHYLCELLULOSE 603 [II]
HYPROMELLOSE 2910 (3 CPS)
HYPROMELLOSE 2910 (3 MPA.S)
HYPROMELLOSE 3CP
HYPROMELLOSE 603
HYPROMELLOSE E3

Brand / Trade Names

BENECEL HPMC E3
METHOCEL E3
PHARMACOAT 603

NDC Products Containing HYPROMELLOSE 2910 (3 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.
→ ATLANTIC BIOLOGICALS CORP. 2
→ Accord Healthcare Inc. 3
→ Accord Healthcare, Inc. 2
→ Actavis Pharma, Inc. 2
→ AiPing Pharmaceutical, Inc. 1
→ Amneal Pharmaceuticals of New York LLC 9
→ BETTER LIVING BRANDS LLC. 1
→ Better Living Brands, LLC 1
→ Camber Pharmaceuticals, Inc. 22
→ Cintex Services, LLC 1
→ Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. 5
→ Hikma Pharmaceuticals USA Inc 2
→ KROGER COMPANY 1
→ Macleods Pharmaceuticals Limited 8
→ Major Pharmaceuticals 11
→ Marlex Pharmaceuticals, Inc. 2
→ Merck Sharp & Dohme LLC 1
→ Mylan Pharmaceuticals Inc. 3
→ NCS HealthCare of KY, LLC dba Vangard Labs 12
→ NorthStar Rx LLC 9
→ Padagis US LLC 4
→ Rising Pharma Holdings, Inc. 10
→ SAFEWAY 1
→ Sandoz Inc 5
→ Supernus Pharmaceuticals 2
→ TARGET CORPORATION 1
→ Teva Pharmaceuticals USA, Inc. 52
→ Teva Pharmaceuticals, Inc. 10
→ Torrent Pharmaceuticals Limited 8
→ Unichem Pharmaceuticals (USA), Inc. 2
→ Upsher-Smith Laboratories, LLC 3
→ WALGREEN CO. 2
→ Walgreens 1
→ Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. 1

ATLANTIC BIOLOGICALS CORP.

NDC Product
Human Prescription Drug

Atovaquone
NDC 17856-0631

Generic Name
Atovaquone
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Atovaquone
NDC 17856-8631

Generic Name
Atovaquone
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing

Accord Healthcare Inc.

NDC Product
Human Prescription Drug

Tadalafil
NDC 16729-369

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

Tadalafil
NDC 16729-370

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

Tadalafil
NDC 16729-372

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

Accord Healthcare, Inc.

NDC Product
Human Prescription Drug

Eplerenone
NDC 16729-293

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

Eplerenone
NDC 16729-294

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

Actavis Pharma, Inc.

NDC Product
Human Prescription Drug

Budesonide
NDC 0591-2510

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

Trospium Chloride
NDC 0591-3636

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

AiPing Pharmaceutical, Inc.

NDC Product
Human Prescription Drug

Sevelamer Carbonate
NDC 11788-116

Generic Name
Sevelamer Carbonate
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Amneal Pharmaceuticals of New York LLC

NDC Product
Human Prescription Drug

Bupropion Hydrochloride
NDC 0115-5445

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

Fenofibrate
NDC 0115-5511

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

Fenofibrate
NDC 0115-5522

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

BETTER LIVING BRANDS LLC.

NDC Product
Human Otc Drug

Acetaminophen
NDC 21130-356

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

Better Living Brands, LLC

NDC Product
Human Otc Drug

Ibuprofen And Diphenhydramine Citrate
NDC 21130-228

Generic Name
Ibuprofen And Diphenhydramine Citrate
Dosage Form
Tablet, Coated
Route
Oral
Marketing
ANDA
Active Listing

Camber Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Oxcarbazepine
NDC 31722-023

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

Oxcarbazepine
NDC 31722-024

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

Oxcarbazepine
NDC 31722-025

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

Eplerenone
NDC 31722-049

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

Eplerenone
NDC 31722-050

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

Lurasidone Hydrochloride
NDC 31722-080

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

Lurasidone Hydrochloride
NDC 31722-081

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

Lurasidone Hydrochloride
NDC 31722-082

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

Lurasidone Hydrochloride
NDC 31722-083

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

Lurasidone Hydrochloride
NDC 31722-084

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

Metoprolol Succinate
NDC 31722-589

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

Metoprolol Succinate
NDC 31722-590

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

Metoprolol Succinate
NDC 31722-591

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

Metoprolol Succinate
NDC 31722-592

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

Rufinamide
NDC 31722-598

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

Rufinamide
NDC 31722-599

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

Atovaquone
NDC 31722-629

Generic Name
Atovaquone
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Abacavir And Lamivudine
NDC 31722-838

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

Eltrombopag
NDC 31722-841

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

Eltrombopag
NDC 31722-842

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

Eltrombopag
NDC 31722-843

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

Eltrombopag
NDC 31722-844

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

Cintex Services, LLC

NDC Product
Human Prescription Drug

Diclofenac Potassium
NDC 24470-924

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

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

NDC Product
Human Prescription Drug

Nystatin
NDC 23155-051

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

Benazepril Hydrochloride
NDC 23155-749

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

Benazepril Hydrochloride
NDC 23155-750

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

Benazepril Hydrochloride
NDC 23155-751

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

Benazepril Hydrochloride
NDC 23155-752

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

Hikma Pharmaceuticals USA Inc

NDC Product
Human Prescription Drug

Prucalopride
NDC 0054-0749

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

Prucalopride
NDC 0054-0750

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

KROGER COMPANY

NDC Product
Human Otc Drug

Ibuprofen Pm
NDC 30142-278

Generic Name
Ibuprofen And Diphenhydramine Citrate
Dosage Form
Tablet, Coated
Route
Oral
Marketing
ANDA
Active Listing

Macleods Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Fenofibrate
NDC 33342-339

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

Fenofibrate
NDC 33342-340

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

Metformin Hydrochloride
NDC 33342-378

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

Diltiazem Hydrochloride
NDC 33342-521

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

Diltiazem Hydrochloride
NDC 33342-522

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

Diltiazem Hydrochloride
NDC 33342-523

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

Diltiazem Hydrochloride
NDC 33342-524

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

Diltiazem Hydrochloride
NDC 33342-525

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

Major Pharmaceuticals

NDC Product
Human Prescription Drug

Pantoprazole Sodium
NDC 0904-6474

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

Pantoprazole Sodium
NDC 0904-6870

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

Levetiracetam
NDC 0904-7123

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

Levetiracetam
NDC 0904-7124

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

Levetiracetam
NDC 0904-7125

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

Fenofibrate
NDC 0904-7161

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

Labetalol Hydrochloride
NDC 0904-7451

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

Labetalol Hydrochloride
NDC 0904-7452

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

Labetalol Hydrochloride
NDC 0904-7453

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

Fenofibrate
NDC 0904-7480

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

Ramelteon
NDC 0904-7494

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

Marlex Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Methocarbamol Tablets, Usp, 500 Mg
NDC 10135-722

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

Methocarbamol Tablets, Usp, 750 Mg
NDC 10135-723

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

Merck Sharp & Dohme LLC

NDC Product
Human Prescription Drug

Zepatier
NDC 0006-3074

Generic Name
Elbasvir And Grazoprevir
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing

Mylan Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Imatinib Mesylate
NDC 0378-2245

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

Imatinib Mesylate
NDC 0378-2246

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

Budesonide
NDC 0378-4500

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

NCS HealthCare of KY, LLC dba Vangard Labs

NDC Product
Human Prescription Drug

Pantoprazole Sodium
NDC 0615-8113

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

Carvedilol
NDC 0615-8387

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

Carvedilol
NDC 0615-8388

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

Carvedilol
NDC 0615-8389

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

Carvedilol
NDC 0615-8390

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

Labetalol Hydrochloride
NDC 0615-8512

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

Labetalol Hydrochloride
NDC 0615-8513

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

Fenofibrate
NDC 0615-8530

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

Topiramate
NDC 0615-8593

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

Topiramate
NDC 0615-8594

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

Topiramate
NDC 0615-8595

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

Esomeprazole Magnesium
NDC 0615-8628

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

NorthStar Rx LLC

NDC Product
Human Prescription Drug

Paroxetine
NDC 16714-182

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

Paroxetine
NDC 16714-183

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

Paroxetine
NDC 16714-184

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

Lansoprazole
NDC 16714-185

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

Lansoprazole
NDC 16714-186

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

Cefprozil
NDC 16714-398

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

Cefprozil
NDC 16714-399

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

Padagis US LLC

NDC Product
Human Prescription Drug

Hydromorphone Hydrochloride
NDC 0574-0293

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

Hydromorphone Hydrochloride
NDC 0574-0294

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

Hydromorphone Hydrochloride
NDC 0574-0295

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

Hydromorphone Hydrochloride
NDC 0574-0297

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

Rising Pharma Holdings, Inc.

NDC Product
Human Prescription Drug

Hydroxyzine Hydrochloride
NDC 16571-113

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

Hydroxyzine Hydrochloride
NDC 16571-114

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

Hydroxyzine Hydrochloride
NDC 16571-115

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

Memantine Hydrochloride
NDC 16571-852

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

Memantine Hydrochloride
NDC 16571-853

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

Memantine Hydrochloride
NDC 16571-854

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

Memantine Hydrochloride
NDC 16571-855

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

Pentoxifylline
NDC 16571-856

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

Indapamide
NDC 16571-875

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

Indapamide
NDC 16571-876

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

SAFEWAY

Sandoz Inc

NDC Product
Human Prescription Drug

Clarithromycin
NDC 0781-1961

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

Clarithromycin
NDC 0781-1962

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

Pirfenidone
NDC 0781-2158

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

Sitagliptin And Metformin Hydrochloride
NDC 0781-5801

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

Sitagliptin And Metformin Hydrochloride
NDC 0781-5802

Generic Name
Sitagliptin And Metformin Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Supernus Pharmaceuticals

NDC Product
Human Prescription Drug

Gocovri
NDC 17772-085

Generic Name
Amantadine
Dosage Form
Capsule, Coated Pellets
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Gocovri
NDC 17772-170

Generic Name
Amantadine
Dosage Form
Capsule, Coated Pellets
Route
Oral
Marketing
NDA
Active Listing

TARGET CORPORATION

Teva Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Moexipril Hydrochloride
NDC 0093-0017

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

Carvedilol
NDC 0093-0051

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

Carvedilol
NDC 0093-0135

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

Ketorolac Tromethamine
NDC 0093-0314

Generic Name
Ketorolac Tromethamine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0093-0314

Generic Name
Ketorolac Tromethamine
Dosage Form
Tablet, Film Coated
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Cefprozil
NDC 0093-1078

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

Tri-lo-sprintec
NDC 0093-2140

Generic Name
Norgestimate And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Cephalexin
NDC 0093-2238

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

Cephalexin
NDC 0093-2240

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

Amoxicillin And Clavulanate Potassium
NDC 0093-2274

Generic Name
Amoxicillin And Clavulanate Potassium
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Amoxicillin And Clavulanate Potassium
NDC 0093-2275

Generic Name
Amoxicillin And Clavulanate Potassium
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Amoxicillin And Clavulanate Potassium
NDC 0093-2277

Generic Name
Amoxicillin And Clavulanate Potassium
Dosage Form
Powder, For Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Amoxicillin And Clavulanate Potassium
NDC 0093-2279

Generic Name
Amoxicillin And Clavulanate Potassium
Dosage Form
Powder, For Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Risedronate Sodium
NDC 0093-3098

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

Risedronate Sodium
NDC 0093-3099

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

Risedronate Sodium
NDC 0093-3100

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

Camrese
NDC 0093-3134

Generic Name
Levonorgestrel / Ethinyl Estradiol And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Reclipsen 28 Day
NDC 0093-3304

Generic Name
Desogestrel And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Hydroxyzine Hydrochloride
NDC 0093-5060

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

Hydroxyzine Hydrochloride
NDC 0093-5061

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

Hydroxyzine Hydrochloride
NDC 0093-5062

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

Moexipril Hydrochloride
NDC 0093-5150

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

Almotriptan Malate
NDC 0093-5260

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

Almotriptan Malate
NDC 0093-5261

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

Mimvey
NDC 0093-5455

Generic Name
Estradiol And Norethindrone Acetate
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Rivelsa
NDC 0093-6031

Generic Name
Levonorgestrel/ethinyl Estradiol And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Camrese Lo
NDC 0093-6148

Generic Name
Levonorgestrel/ethinyl Estradiol And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Carvedilol
NDC 0093-7295

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

Carvedilol
NDC 0093-7296

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

Capecitabine
NDC 0093-7473

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

Capecitabine
NDC 0093-7474

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

Erlotinib
NDC 0093-7663

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

Erlotinib
NDC 0093-7664

Generic Name
Erlotinib
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0093-8117

Generic Name
Famciclovir
Dosage Form
Tablet, Film Coated
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Famciclovir
NDC 0093-8117

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

Famciclovir
NDC 0093-8118

Generic Name
Famciclovir
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0093-8118

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

NDC 0093-8119

Generic Name
Famciclovir
Dosage Form
Tablet, Film Coated
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Famciclovir
NDC 0093-8119

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

Quetiapine
NDC 0093-8162

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

Quetiapine
NDC 0093-8163

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

Quetiapine
NDC 0093-8164

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

Quetiapine
NDC 0093-8165

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

Quetiapine
NDC 0093-8166

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

Eletriptan Hydrobromide
NDC 0093-8310

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

Eletriptan Hydrobromide
NDC 0093-8311

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

Lessina
NDC 0555-9014

Generic Name
Levonorgestrel And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Portia
NDC 0555-9020

Generic Name
Levonorgestrel And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Apri 28 Day
NDC 0555-9043

Generic Name
Desogestrel And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Kariva
NDC 0555-9050

Generic Name
Desogestrel/ethinyl Estradiol And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Velivet Triphasic Regimen
NDC 0555-9051

Generic Name
Desogestrel And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Jolessa
NDC 0555-9123

Generic Name
Levonorgestrel / Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
NDA AUTHORIZED GENERIC
Active Listing

Teva Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Ticagrelor
NDC 0480-2688

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

Ticagrelor
NDC 0480-2695

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

Alvaiz
NDC 0480-3274

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

Alvaiz
NDC 0480-3275

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

Alvaiz
NDC 0480-3276

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

Pazopanib
NDC 0480-4184

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

Torrent Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Pantoprazole Sodium
NDC 13668-096

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

Carbamazepine
NDC 13668-284

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

Carbamazepine
NDC 13668-285

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

Carbamazepine
NDC 13668-286

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

Pantoprazole Sodium
NDC 13668-429

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

Erythromycin
NDC 13668-606

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

Erythromycin
NDC 13668-607

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

Pazopanib
NDC 13668-735

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

Unichem Pharmaceuticals (USA), Inc.

NDC Product
Human Prescription Drug

Prasugrel
NDC 29300-301

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

Prasugrel
NDC 29300-302

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

Upsher-Smith Laboratories, LLC

NDC Product
Human Prescription Drug

Fluphenazine Hydrochloride
NDC 24979-137

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

Fluphenazine Hydrochloride
NDC 24979-138

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

Fluphenazine Hydrochloride
NDC 24979-139

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

WALGREEN CO.

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 0363-0361

Generic Name
Esomeprazole Magnesium
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Pseudoephedrine Hydrochloride
NDC 0363-6611

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

Walgreens

NDC Product
Human Otc Drug

Fexofenadine Hcl
NDC 0363-6231

Generic Name
Fexofenadine Hcl
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.

NDC Product
Human Prescription Drug

Protonix Delayed-release
NDC 0008-0844

Generic Name
Pantoprazole Sodium
Dosage Form
Granule, Delayed Release
Route
Oral
Marketing
NDA
Active Listing

External Clinical & Regulatory Resources

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