HYPROMELLOSE 2208 (15000 MPA.S)
UNII Z78RG6M2N2

Substance Identification & Data

This profile provides standardized clinical and technical data for Hypromellose 2208 (15000 Mpa.s), uniquely identified by the FDA Unique Ingredient Identifier (UNII) Z78RG6M2N2.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9004-65-3 and the RxNorm Concept ID (RxCUI) 1300445. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
Z78RG6M2N2
CAS Registry Number
9004-65-3
RxNorm Concept ID
1300445

Detailed Substance Profile

Preferred Name
HYPROMELLOSE 2208 (15000 MPA.S)
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
Z78RG6M2N2
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
C80265
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 2208 (15000 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 (15000 CPS)
HYDROXYPROPYL METHYLCELLULOSE 2208 (11250-21000 CPS)
HYDROXYPROPYL METHYLCELLULOSE 2208 (15000 CPS)
HYPERMELLOSE 2208 (11250 - 21000 CPS)
HYPROMELLOSE 2208 (11250 - 21000 CPS)
HYPROMELLOSE 2208 (15000 CPS)
HYPROMELLOSE 2208 (15000 MPA.S)
HYPROMELLOSE 2208 (15000 MPA.S) [II]
METHOCEL K-15M PREMIUM

Brand / Trade Names

BENECEL HPMC K15M
DEMACOL HK 15M
METHOCEL K15M
METOLOSE 90SH 15000
METOLOSE 90SH 15000SR

NDC Products Containing HYPROMELLOSE 2208 (15000 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 (278), only Active Listings are currently displayed.
→ A-S Medication Solutions 7
→ Alembic Pharmaceuticals Inc. 7
→ Alembic Pharmaceuticals Limited 7
→ American Health Packaging 2
→ Amerisource Bergen 1
→ Apotex Corp. 7
→ Aurohealth LLC 10
→ Aurolab 1
→ Better Living Brands LLC 2
→ Better Living Brands, LLC 1
→ BluePoint Laboratories 3
→ Bryant Ranch Prepack 8
→ Camber Pharmaceuticals, Inc. 3
→ Coupler LLC 2
→ Direct_Rx 1
→ Dr. Reddy's Laboratories Ltd 1
→ Edenbridge Pharmaceuticals LLC. 1
→ Fosun Pharma USA, Inc 4
→ Golden State Medical Supply, Inc. 2
→ Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. 3
→ Ingenus Pharmaceuticals, LLC 7
→ KROGER COMPANY 1
→ Laurus Labs Limited 2
→ Leading Pharma, LLC 2
→ Lupin Pharmaceuticals, Inc. 6
→ Major Pharmaceuticals 5
→ Meijer 1
→ Micro Labs Limited 2
→ NorthStar RxLLC 1
→ OASIS Medical, Inc. 1
→ Oculus Surgical, Inc. 1
→ PD-Rx Pharmaceuticals, Inc. 1
→ Prasco Laboratories 5
→ Preferred Pharmaceuticals Inc. 1
→ Proficient Rx LP 1
→ REMEDYREPACK INC. 3
→ RITE AID CORPORATION 1
→ Sam's West Inc 1
→ Sandoz Inc 2
→ Simpex Pharma Pvt. Ltd 1
→ Solco Healthcare LLC 1
→ SpecGx LLC 7
→ Sun Pharmaceutical Industries, Inc. 2
→ TOPCO ASSOCIATES LLC 1
→ Takeda Pharmaceuticals America, Inc. 4
→ Teva Pharmaceuticals USA, Inc. 3
→ Unichem Pharmaceuticals (USA), Inc. 2
→ VESPYR BRANDS LLC 2
→ WALGREEN CO. 4
→ WALGREENS CO. 1
→ WALMART INC. 1
→ Wal-Mart Stores Inc 1
→ Walgreens 1
→ Whole Foods Market, Inc. 1
→ Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. 13
→ Xiamen LP Pharmaceutical Co., Ltd. 1

A-S Medication Solutions

NDC Product
Human Prescription Drug

Premarin
NDC 50090-0167

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

Premarin
NDC 50090-1853

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

Digoxin
NDC 50090-5642

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

Digoxin
NDC 50090-5862

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

Guanfacine Extended-release
NDC 50090-6493

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

Digoxin
NDC 50090-6588

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

Divalproex Sodium
NDC 50090-7841

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

Alembic Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Pramipexole Dihydrochloride
NDC 62332-154

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

Pramipexole Dihydrochloride
NDC 62332-155

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

Pramipexole Dihydrochloride
NDC 62332-156

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

Pramipexole Dihydrochloride
NDC 62332-157

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

Pramipexole Dihydrochloride
NDC 62332-158

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

Pramipexole Dihydrochloride
NDC 62332-159

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

Pramipexole Dihydrochloride
NDC 62332-160

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

Alembic Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Pramipexole Dihydrochloride
NDC 46708-574

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

Pramipexole Dihydrochloride
NDC 46708-575

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

Pramipexole Dihydrochloride
NDC 46708-576

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

Pramipexole Dihydrochloride
NDC 46708-577

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

Pramipexole Dihydrochloride
NDC 46708-578

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

Pramipexole Dihydrochloride
NDC 46708-579

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

Pramipexole Dihydrochloride
NDC 46708-580

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

American Health Packaging

NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 60687-904

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 60687-915

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

Amerisource Bergen

NDC Product
Human Otc Drug

Guaifenesin And Pseudoephedrine Hcl
NDC 46122-801

Generic Name
Guaifenesin And Pseudoephedrine Hcl
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Apotex Corp.

NDC Product
Human Prescription Drug

Levetiracetam
NDC 60505-3280

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

Levetiracetam
NDC 60505-3517

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

Levetiracetam
NDC 60505-3518

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

Guanfacine Extended-release
NDC 60505-3927

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

Guanfacine Extended-release
NDC 60505-3928

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

Guanfacine Extended-release
NDC 60505-3929

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

Guanfacine Extended-release
NDC 60505-3930

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

Aurohealth LLC

NDC Product
Human Otc Drug

Pseudoephedrine Hcl
NDC 58602-804

Generic Name
Pseudoephedrine Hcl
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Guaifenesin
NDC 58602-810

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

Guaifenesin
NDC 58602-811

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

Guaifenesin And Pseudoephedrine Hcl
NDC 58602-833

Generic Name
Guaifenesin And Pseudoephedrine Hcl
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Guaifenesin And Pseudoephedrine Hcl
NDC 58602-834

Generic Name
Guaifenesin And Pseudoephedrine Hcl
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Guaifenesin
NDC 58602-853

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

Guaifenesin
NDC 58602-864

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

Guaifenesin
NDC 58602-865

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

Aurolab

NDC Product
Human Otc Drug

Aurovisc
NDC 16030-301

Generic Name
Hypromellose Ophthalmic Solution 2% W/v
Dosage Form
Solution
Route
Ophthalmic
Marketing
OTC MONOGRAPH DRUG
Active Listing

Better Living Brands LLC

NDC Product
Human Otc Drug

Pseudoephedrine Hcl
NDC 21130-158

Generic Name
Pseudoephedrine Hcl
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Guaifenesin
NDC 21130-179

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

Better Living Brands, LLC

NDC Product
Human Otc Drug

Mucus Relief Max
NDC 21130-399

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

BluePoint Laboratories

NDC Product
Human Otc Drug

Guaifenesin
NDC 68001-561

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

Divalproex Sodium
NDC 68001-646

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 68001-647

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

Bryant Ranch Prepack

NDC Product
Human Prescription Drug

Clonidine Hydrochloride
NDC 63629-1208

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

Divalproex Sodium
NDC 71335-2535

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

Guanfacine Extended-release
NDC 71335-2852

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

Guanfacine Extended-release
NDC 71335-3005

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

Guanfacine Extended-release
NDC 71335-3078

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

Digoxin
NDC 71335-9610

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

Guanfacine Extended-release
NDC 71335-9750

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

Clonidine Hydrochloride
NDC 72162-1367

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

Camber Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 31722-021

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 31722-022

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

Zileuton
NDC 31722-044

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

Coupler LLC

NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 67046-1595

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 67046-1631

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

Direct_Rx

NDC Product
Human Prescription Drug

Guanfacine Er
NDC 72189-469

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

Dr. Reddy's Laboratories Ltd

NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 55111-534

Generic Name
Divalproex Sodium
Dosage Form
Tablet, Extended Release
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

Fosun Pharma USA, Inc

NDC Product
Human Prescription Drug

Guanfacine
NDC 72266-255

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

Guanfacine
NDC 72266-256

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

Guanfacine
NDC 72266-257

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

Guanfacine
NDC 72266-258

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

Golden State Medical Supply, Inc.

NDC Product
Human Prescription Drug

Levetiracetam Extended-release
NDC 60429-349

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

Levetiracetam Extended-release
NDC 60429-350

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

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

NDC Product
Human Prescription Drug

Felodipine
NDC 23155-048

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

Felodipine
NDC 23155-049

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

Felodipine
NDC 23155-050

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

Ingenus Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Pramipexole Dihydrochloride
NDC 50742-331

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

Pramipexole Dihydrochloride
NDC 50742-332

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

Pramipexole Dihydrochloride
NDC 50742-333

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

Pramipexole Dihydrochloride
NDC 50742-334

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

Pramipexole Dihydrochloride
NDC 50742-335

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

Pramipexole Dihydrochloride
NDC 50742-336

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

Pramipexole Dihydrochloride
NDC 50742-337

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

KROGER COMPANY

NDC Product
Human Otc Drug

Guaifenesin And Pseudoephedrine Hcl
NDC 30142-137

Generic Name
Guaifenesin And Pseudoephedrine Hcl
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Laurus Labs Limited

NDC Product
Human Prescription Drug

Fenofibric Acid Delayed-release
NDC 42385-944

Generic Name
Fenofibric Acid
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Fenofibric Acid Delayed-release
NDC 42385-945

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

Leading Pharma, LLC

NDC Product
Human Prescription Drug

Fenofibric Acid
NDC 69315-281

Generic Name
Fenofibric Acid
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Fenofibric Acid
NDC 69315-282

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

Lupin Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Clonidine Hydrochloride
NDC 68180-606

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

Quetiapine
NDC 68180-612

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

Quetiapine
NDC 68180-613

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

Quetiapine
NDC 68180-614

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

Quetiapine
NDC 68180-615

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

Quetiapine
NDC 68180-616

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

Major Pharmaceuticals

NDC Product
Human Prescription Drug

Quetiapine
NDC 0904-6801

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

Quetiapine
NDC 0904-6802

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

Quetiapine
NDC 0904-6803

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

Quetiapine
NDC 0904-6804

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

Quetiapine
NDC 0904-6805

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

Meijer

NDC Product
Human Otc Drug

Guaifenesin And Pseudoephedrine Hcl
NDC 79481-1002

Generic Name
Guaifenesin And Pseudoephedrine Hcl
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Micro Labs Limited

NDC Product
Human Prescription Drug

Fenofibric Acid
NDC 42571-347

Generic Name
Fenofibric Acid
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Fenofibric Acid
NDC 42571-348

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

NorthStar RxLLC

NDC Product
Human Prescription Drug

Zileuton
NDC 72603-246

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

OASIS Medical, Inc.

NDC Product
Human Otc Drug

Visco Shield Lubricant
NDC 42126-5200

Generic Name
Hypromellose 2208 (15000 Mpa.s)
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
OTC MONOGRAPH DRUG
Active Listing

Oculus Surgical, Inc.

NDC Product
Human Otc Drug

Improvue Lubricant
NDC 62144-5510

Generic Name
Hypromellose 2208 (15000 Mpa.s)
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
OTC MONOGRAPH DRUG
Active Listing

PD-Rx Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Ciprofloxacin
NDC 43063-547

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

Prasco Laboratories

NDC Product
Human Prescription Drug

Conjugated Estrogens
NDC 66993-295

Generic Name
Estrogens, Conjugated
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Conjugated Estrogens
NDC 66993-296

Generic Name
Estrogens, Conjugated
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Conjugated Estrogens
NDC 66993-297

Generic Name
Estrogens, Conjugated
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Conjugated Estrogens
NDC 66993-298

Generic Name
Estrogens, Conjugated
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Conjugated Estrogens
NDC 66993-299

Generic Name
Estrogens, Conjugated
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing

Preferred Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 68788-4100

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

Proficient Rx LP

NDC Product
Human Prescription Drug

Etodolac
NDC 71205-140

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

REMEDYREPACK INC.

NDC Product
Human Prescription Drug

Guanfacine Extended-release
NDC 70518-4266

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

Divalproex Sodium
NDC 70518-4553

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 70518-4557

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

RITE AID CORPORATION

NDC Product
Human Otc Drug

Guaifenesin
NDC 11822-4260

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

Sam's West Inc

NDC Product
Human Otc Drug

Guaifenesin
NDC 68196-960

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

Sandoz Inc

NDC Product
Human Prescription Drug

Fluvastatin Sodium Er
NDC 0781-8017

Generic Name
Fluvastatin Sodium
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Lescol Xl
NDC 66758-211

Generic Name
Fluvastatin Sodium
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
NDA
Active Listing

Simpex Pharma Pvt. Ltd

NDC Product
Human Otc Drug

Simpex Bisacodyl Laxative
NDC 76457-003

Generic Name
Bisacodyl
Dosage Form
Tablet, Coated
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Solco Healthcare LLC

NDC Product
Human Prescription Drug

Clonidine Hydrochloride
NDC 43547-435

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

SpecGx LLC

NDC Product
Human Prescription Drug

Methylphenidate Hydrochloride
NDC 0406-1445

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

Methylphenidate Hydrochloride
NDC 0406-1473

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

Morphine Sulfate
NDC 0406-8315

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

Morphine Sulfate
NDC 0406-8320

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

Morphine Sulfate
NDC 0406-8330

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

Morphine Sulfate
NDC 0406-8380

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

Morphine Sulfate
NDC 0406-8390

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

Sun Pharmaceutical Industries, Inc.

NDC Product
Human Prescription Drug

Digoxin
NDC 57664-437

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

Digoxin
NDC 57664-441

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

TOPCO ASSOCIATES LLC

NDC Product
Human Otc Drug

Guaifenesin
NDC 76162-031

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

Takeda Pharmaceuticals America, Inc.

NDC Product
Human Prescription Drug

Intuniv
NDC 54092-513

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

Intuniv
NDC 54092-515

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

Intuniv
NDC 54092-517

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

Intuniv
NDC 54092-519

Generic Name
Guanfacine
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
NDA
Active Listing

Teva Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Etodolac
NDC 0093-1118

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

Etodolac
NDC 0093-1122

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

Etodolac
NDC 0093-7172

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

Unichem Pharmaceuticals (USA), Inc.

NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 29300-380

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 29300-381

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

VESPYR BRANDS LLC

NDC Product
Human Otc Drug

Guaifenesin
NDC 71179-002

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

WALGREEN CO.

NDC Product
Human Otc Drug

Guaifenesin
NDC 0363-0028

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

Guaifenesin
NDC 0363-0033

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

Guaifenesin And Pseudoephedrine Hcl
NDC 0363-0134

Generic Name
Guaifenesin And Pseudoephedrine Hcl
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Guaifenesin And Pseudoephedrine Hcl
NDC 0363-9946

Generic Name
Guaifenesin And Pseudoephedrine Hcl
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

WALGREENS CO.

NDC Product
Human Otc Drug

Extra Strength Acetaminophen
NDC 0363-9084

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

WALMART INC.

NDC Product
Human Otc Drug

Extra Strength Pain Reliever Pm
NDC 79903-053

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

Wal-Mart Stores Inc

NDC Product
Human Otc Drug

Extra Strength Acetaminophen
NDC 79903-032

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

Walgreens

NDC Product
Human Otc Drug

Itch Relief Gel
NDC 0363-0353

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

Whole Foods Market, Inc.

Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.

NDC Product
Human Prescription Drug

Pristiq Extended-release
NDC 0008-1210

Generic Name
Desvenlafaxine Succinate
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Pristiq Extended-release
NDC 0008-1211

Generic Name
Desvenlafaxine Succinate
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Pristiq Extended-release
NDC 0008-1222

Generic Name
Desvenlafaxine Succinate
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Premarin
NDC 0046-1100

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

Premarin
NDC 0046-1101

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

Premarin
NDC 0046-1102

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

Premarin
NDC 0046-1103

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

Premarin
NDC 0046-1104

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

Prempro
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 Drug

Prempro
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 Drug

Prempro
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 Drug

Prempro
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 Drug

Premphase
NDC 0046-2575

Generic Name
Conjugated Estrogens And Medroxyprogesterone Acetate
Dosage Form
Kit
Route
N/A
Marketing
NDA
Active Listing

Xiamen LP Pharmaceutical Co., Ltd.

NDC Product
Human Prescription Drug

Clonidine Hydrochloride
NDC 71034-001

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

External Clinical & Regulatory Resources

CAS
Common Chemistry
NCATS
Inxight Drugs
NLM
DailyMed Products
NCATS
GSRS Full Record
NIH
NCI Thesaurus