HYPROMELLOSE 2208 (4000 MPA.S)
UNII 39J80LT57T

Substance Identification & Data

This profile provides standardized clinical and technical data for Hypromellose 2208 (4000 Mpa.s), uniquely identified by the FDA Unique Ingredient Identifier (UNII) 39J80LT57T.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9004-65-3 and the RxNorm Concept ID (RxCUI) 1300447. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
39J80LT57T
CAS Registry Number
9004-65-3
RxNorm Concept ID
1300447

Detailed Substance Profile

Preferred Name
HYPROMELLOSE 2208 (4000 MPA.S)
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
39J80LT57T
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 (4000 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

HYPROMELLOSE 2208 (4000 CPS)
HYPROMELLOSE 2208 (4000 MPA.S)

Brand / Trade Names

BENECEL HPMC K4M
BENECEL MP843
METHOCEL K4M
METHOCEL K-4M PREMIUM
METOLOSE 90SH 4000
METOLOSE 90SH 4000SR

NDC Products Containing HYPROMELLOSE 2208 (4000 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 (244), only Active Listings are currently displayed. Display is limited to the first 200 products.
→ 7-Eleven 2
→ A-S Medication Solutions 9
→ ADVANCED FIRST AID, INC. 1
→ Accord Healthcare Inc. 5
→ Accord Healthcare, Inc. 2
→ Allergan, Inc. 1
→ American Health Packaging 1
→ Apotex Corp. 1
→ Ascend Laboratories, LLC 9
→ Asclemed USA, Inc. 1
→ Aurobindo Pharma Limited 25
→ Aurohealth LLC 5
→ AvKARE 1
→ AvPAK 1
→ Belmora LLC 1
→ Better Living Brands LLC 1
→ Better Living Brands, LLC 1
→ BluePoint Laboratories 6
→ Bryant Ranch Prepack 36
→ CVS Pharmacy 2
→ Camber Pharmaceuticals, Inc. 6
→ Coupler LLC 1
→ Cranbury Pharmaceuticals, LLC 4
→ Direct_Rx 3
→ Dr. Reddy's Laboratories Inc. 12
→ Golden State Medical Supply, Inc. 1
→ KROGER COMPANY 1
→ NorthStar RxLLC 2
→ NuCare Pharmaceuticals, Inc. 3
→ NuCare Pharmaceuticals,Inc. 2
→ Oceanside Pharmaceuticals 2
→ Oryza Pharmaceuticals, Inc 4
→ PD-Rx Pharmaceuticals, Inc. 9
→ Padagis Israel Pharmaceuticals Ltd 1
→ Prasco Laboratories 1
→ Preferred Pharmaceuticals Inc 1
→ Proficient Rx LP 3
→ REMEDYREPACK INC. 5
→ Randob Labs., Ltd. 1
→ Redpharm Drug 1
→ SAM'S WEST INC 1
→ Safecor Health, LLC 2
→ Solco Healthcare U.S., LLC 4
→ Strategic Sourcing Services, LLC 2
→ Sun Pharmaceutical Industries, Inc. 3
→ Teva Pharmaceuticals USA, Inc. 1
→ Torrent Pharmaceuticals Limited 2
→ Unichem Pharmaceuticals (USA), Inc. 9
→ Upsher-Smith Laboratories, LLC 1
→ WALGREEN CO. 1

7-Eleven

NDC Product
Human Otc Drug

Childrens Ibuprofen
NDC 10202-150

Generic Name
Ibuprofen
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Childrens Ibuprofen
NDC 10202-711

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

A-S Medication Solutions

NDC Product
Human Prescription Drug

Estrace
NDC 50090-2321

Generic Name
Estradiol
Dosage Form
Cream
Route
Vaginal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Estradiol
NDC 50090-3327

Generic Name
Estradiol
Dosage Form
Cream
Route
Vaginal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Estradiol
NDC 50090-3645

Generic Name
Estradiol
Dosage Form
Cream
Route
Vaginal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 50090-6448

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

Metoprolol Succinate
NDC 50090-6488

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

Metoprolol Succinate
NDC 50090-6489

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

Estradiol Vaginal
NDC 50090-6811

Generic Name
Estradiol
Dosage Form
Cream
Route
Vaginal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Estradiol Vaginal
NDC 50090-7266

Generic Name
Estradiol
Dosage Form
Cream
Route
Vaginal
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

ADVANCED FIRST AID, INC.

NDC Product
Human Otc Drug

Ibuprofen
NDC 67060-001

Generic Name
Ibuprofen 200mg
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Accord Healthcare Inc.

NDC Product
Human Prescription Drug

Quetiapine Fumarate
NDC 16729-095

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

Quetiapine Fumarate
NDC 16729-096

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

Quetiapine Fumarate
NDC 16729-097

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

Quetiapine Fumarate
NDC 16729-109

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

Accord Healthcare, Inc.

NDC Product
Human Prescription Drug

Carbidopa And Levodopa
NDC 16729-078

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

Carbidopa And Levodopa
NDC 16729-079

Generic Name
Carbidopa And Levodopa
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Allergan, Inc.

NDC Product
Human Prescription Drug

Estrace
NDC 0430-3754

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

American Health Packaging

NDC Product
Human Prescription Drug

Mesalamine
NDC 60687-650

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

Apotex Corp.

NDC Product
Human Prescription Drug

Alfuzosin Hydrochloride
NDC 60505-2850

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

Ascend Laboratories, LLC

NDC Product
Human Prescription Drug

Minocycline Hydrochloride
NDC 67877-436

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

Minocycline Hydrochloride
NDC 67877-437

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

Minocycline Hydrochloride
NDC 67877-438

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

Minocycline Hydrochloride
NDC 67877-576

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

Minocycline Hydrochloride
NDC 67877-577

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

Minocycline Hydrochloride
NDC 67877-578

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

Minocycline Hydrochloride
NDC 67877-643

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

Minocycline Hydrochloride
NDC 67877-644

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

Mesalamine
NDC 67877-717

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

Asclemed USA, Inc.

NDC Product
Human Prescription Drug

Alprazolam
NDC 76420-651

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

Aurobindo Pharma Limited

NDC Product
Human Prescription Drug

Ibuprofen
NDC 59651-032

Generic Name
Ibuprofen Oral
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
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
Drug For Further Processing

NDC 65862-454

Generic Name
Alprazolam
Dosage Form
Tablet, Extended Release
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Alprazolam
NDC 65862-454

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

Alprazolam
NDC 65862-455

Generic Name
Alprazolam
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 65862-455

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

NDC 65862-456

Generic Name
Alprazolam
Dosage Form
Tablet, Extended Release
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Alprazolam
NDC 65862-456

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

Alprazolam
NDC 65862-457

Generic Name
Alprazolam
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 65862-457

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

NDC 65862-554

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

Minocycline Hydrochloride
NDC 65862-554

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

Minocycline Hydrochloride
NDC 65862-556

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

NDC 65862-556

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

NDC 65862-558

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

Minocycline Hydrochloride
NDC 65862-558

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

Fesoterodine Fumarate
NDC 65862-766

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 65862-767

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

Quetiapine Fumarate
NDC 65862-873

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

Quetiapine Fumarate
NDC 65862-874

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

Quetiapine Fumarate
NDC 65862-875

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

Quetiapine Fumarate
NDC 65862-876

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

Quetiapine Fumarate
NDC 65862-877

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

Aurohealth LLC

NDC Product
Human Otc Drug

Childrens Ibuprofen
NDC 58602-002

Generic Name
Ibuprofen
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Childrens Ibuprofen
NDC 58602-003

Generic Name
Ibuprofen
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Childrens Ibuprofen
NDC 58602-008

Generic Name
Ibuprofen
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Infants Ibuprofen
NDC 58602-227

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

AvKARE

NDC Product
Human Prescription Drug

Estradiol Vaginal
NDC 42291-426

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

AvPAK

NDC Product
Human Prescription Drug

Mesalamine
NDC 50268-577

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

Belmora LLC

NDC Product
Human Otc Drug

Childrens Flanax Oral
NDC 27854-777

Generic Name
Ibuprofen
Dosage Form
Suspension
Route
Oral
Marketing
ANDA
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

Better Living Brands, LLC

NDC Product
Human Otc Drug

Childrens Ibuprofen
NDC 21130-216

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

BluePoint Laboratories

NDC Product
Human Otc Drug

Childrens Ibuprofen
NDC 68001-521

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

Quetiapine
NDC 68001-598

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

Quetiapine
NDC 68001-599

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

Quetiapine
NDC 68001-600

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

Quetiapine
NDC 68001-601

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

Quetiapine
NDC 68001-602

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

Bryant Ranch Prepack

NDC Product
Human Prescription Drug

Donepezil Hydrochloride
NDC 63629-8483

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

Estradiol Vaginal
NDC 63629-8654

Generic Name
Estradiol
Dosage Form
Cream
Route
Vaginal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Estradiol
NDC 63629-8713

Generic Name
Estradiol
Dosage Form
Cream
Route
Vaginal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Minocycline Hydrochloride
NDC 63629-9208

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

Minocycline Hydrochloride
NDC 63629-9209

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

Minocycline Hydrochloride
NDC 63629-9210

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

Minocycline Hydrochloride
NDC 63629-9211

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

Minocycline Hydrochloride
NDC 63629-9212

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

Minocycline Hydrochloride
NDC 63629-9213

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

Minocycline Hydrochloride
NDC 63629-9214

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

Minocycline Hydrochloride
NDC 63629-9215

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

Nifedipine
NDC 71335-0744

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

Alprazolam
NDC 71335-1669

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

Alprazolam
NDC 71335-1839

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

Minocycline Hydrochloride
NDC 71335-2201

Generic Name
Minocycline Hydrochloride
Dosage Form
Tablet, Film Coated, 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

Quetiapine
NDC 71335-2641

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

Minocycline Hydrochloride
NDC 71335-2710

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

Minocycline Hydrochloride
NDC 71335-2711

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

Estradiol Vaginal
NDC 71335-2831

Generic Name
Estradiol
Dosage Form
Cream
Route
Vaginal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Minocycline Hydrochloride
NDC 71335-2904

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

Donepezil Hydrochloride
NDC 72162-1276

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

Estradiol Vaginal
NDC 72162-1389

Generic Name
Estradiol
Dosage Form
Cream
Route
Vaginal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Minocycline Hydrochloride
NDC 72162-1838

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

Minocycline Hydrochloride
NDC 72162-1839

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

Minocycline Hydrochloride
NDC 72162-1840

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

Minocycline Hydrochloride
NDC 72162-1852

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

Minocycline Hydrochloride
NDC 72162-1853

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

Minocycline Hydrochloride
NDC 72162-1854

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

Minocycline Hydrochloride
NDC 72162-1867

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

Minocycline Hydrochloride
NDC 72162-1868

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

Nifedipine
NDC 72162-2534

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

Nifedipine
NDC 72162-2535

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

Nifedipine
NDC 72162-2536

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

Darifenacin
NDC 72162-2570

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

Darifenacin
NDC 72162-2571

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

CVS Pharmacy

NDC Product
Human Otc Drug

Guaifenesin 600 Mg
NDC 51316-008

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

Guaifenesin And Dextromethorphan Hbr
NDC 51316-009

Generic Name
Guaifenesin And Dextromethorphan Hbr
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

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

Gabapentin
NDC 31722-091

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

Gabapentin
NDC 31722-092

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

Coupler LLC

NDC Product
Human Prescription Drug

Quetiapine
NDC 67046-1623

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

Cranbury Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 27808-302

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

Metoprolol Succinate
NDC 27808-303

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

Metoprolol Succinate
NDC 27808-304

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

Metoprolol Succinate
NDC 27808-305

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

Direct_Rx

NDC Product
Human Prescription Drug

Quetiapine Fumarate Er
NDC 72189-481

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

Quetiapine Fumarate Er
NDC 72189-482

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

Quetiapine Fumarate Er
NDC 72189-483

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

Dr. Reddy's Laboratories Inc.

NDC Product
Human Otc Drug

Guaifenesin 600 Mg
NDC 43598-008

Generic Name
Guaifenesin
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 43598-008

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

NDC 43598-009

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

Guaifenesin 1200 Mg
NDC 43598-009

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

Guaifenesin 1200 Mg
NDC 43598-108

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

Guaifenesin 600 Mg
NDC 43598-110

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

Guaifenesin And Dextromethorphan Hbr
NDC 43598-114

Generic Name
Guaifenesin And Dextromethorphan Hbr
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 43598-114

Generic Name
Guaifenesin And Dextromethorphan Hbr
Dosage Form
Tablet, Extended Release
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing

NDC 43598-115

Generic Name
Guaifenesin And Dextromethorphan Hbr
Dosage Form
Tablet, Extended Release
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Otc Drug

Guaifenesin And Dextromethorphan Hbr
NDC 43598-115

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

Guaifenesin And Dextromethorphan Hbr
NDC 43598-231

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

Guaifenesin And Dextromethorphan Hbr
NDC 43598-232

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

Golden State Medical Supply, Inc.

NDC Product
Human Prescription Drug

Donepezil Hydrochloride
NDC 51407-320

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

KROGER COMPANY

NDC Product
Human Otc Drug

Childrens Ibuprofen
NDC 30142-281

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

NorthStar RxLLC

NDC Product
Human Prescription Drug

Fesoterodine Fumarate
NDC 72603-413

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 72603-414

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

NuCare Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Estradiol Vaginal
NDC 68071-3796

Generic Name
Estradiol
Dosage Form
Cream
Route
Vaginal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 68071-3943

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

Metoprolol Succinate
NDC 68071-3965

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

NuCare Pharmaceuticals,Inc.

NDC Product
Human Prescription Drug

Nifedipine
NDC 68071-2838

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

Ibuprofen
NDC 68071-3589

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

Oceanside Pharmaceuticals

NDC Product
Human Prescription Drug

Nifedipine
NDC 68682-108

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

Nifedipine
NDC 68682-109

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

Oryza Pharmaceuticals, Inc

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 72516-030

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

Metoprolol Succinate
NDC 72516-031

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

Metoprolol Succinate
NDC 72516-032

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

Metoprolol Succinate
NDC 72516-033

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

PD-Rx Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 72789-497

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

Minocycline Hydrochloride
NDC 72789-523

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

Minocycline Hydrochloride
NDC 72789-524

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

Minocycline Hydrochloride
NDC 72789-525

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

Minocycline Hydrochloride
NDC 72789-526

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

Minocycline Hydrochloride
NDC 72789-527

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

Minocycline Hydrochloride
NDC 72789-528

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

Minocycline Hydrochloride
NDC 72789-529

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

Minocycline Hydrochloride
NDC 72789-530

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

Padagis Israel Pharmaceuticals Ltd

NDC Product
Human Prescription Drug

Estradiol Vaginal
NDC 45802-097

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

Prasco Laboratories

NDC Product
Human Prescription Drug

Estradiol Vaginal Cream
NDC 66993-002

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

Preferred Pharmaceuticals Inc

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 68788-8448

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

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

Donepezil Hydrochloride
NDC 71205-948

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

REMEDYREPACK INC.

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 70518-4090

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

Metoprolol Succinate
NDC 70518-4190

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

Quetiapine
NDC 70518-4430

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

Quetiapine
NDC 70518-4437

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

Guanfacine
NDC 70518-4539

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

Randob Labs., Ltd.

NDC Product
Human Otc Drug

Childrens Ibuprofen
NDC 52412-911

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

Redpharm Drug

NDC Product
Human Prescription Drug

Nifedipine
NDC 67296-2170

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

SAM'S WEST INC

NDC Product
Human Otc Drug

Members Mark Mucus Relief Dm
NDC 68196-999

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

Safecor Health, LLC

NDC Product
Human Prescription Drug

Carbidopa And Levodopa
NDC 48433-015

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

Carbidopa And Levodopa
NDC 48433-016

Generic Name
Carbidopa And Levodopa
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

Strategic Sourcing Services, LLC

NDC Product
Human Otc Drug

Guaifenesin 600 Mg
NDC 70677-1257

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

Guaifenesin 1200 Mg
NDC 70677-1258

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

Sun Pharmaceutical Industries, Inc.

NDC Product
Human Prescription Drug

Venlafaxine Hydrochloride
NDC 47335-758

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

Venlafaxine Hydrochloride
NDC 47335-759

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

Venlafaxine Hydrochloride
NDC 47335-760

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

Teva Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Estradiol
NDC 0093-3541

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

Torrent Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Darifenacin
NDC 13668-202

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

Darifenacin
NDC 13668-203

Generic Name
Darifenacin
Dosage Form
Tablet, Extended 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
NDC Product
Human Prescription Drug

Guanfacine
NDC 29300-460

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

Guanfacine
NDC 29300-461

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

Guanfacine
NDC 29300-462

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

Guanfacine
NDC 29300-463

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

Upsher-Smith Laboratories, LLC

NDC Product
Human Prescription Drug

Donepezil Hydrochloride
NDC 24979-004

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

WALGREEN CO.

NDC Product
Human Otc Drug

Childrens Ibuprofen
NDC 0363-8901

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

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