HYDROGENATED COTTONSEED OIL
UNII Z82Y2C65EA

Substance Identification & Data

This profile provides standardized clinical and technical data for Hydrogenated Cottonseed Oil, uniquely identified by the FDA Unique Ingredient Identifier (UNII) Z82Y2C65EA.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 68334-00-9 and the RxNorm Concept ID (RxCUI) 1309478. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
Z82Y2C65EA
CAS Registry Number
68334-00-9
RxNorm Concept ID
1309478

Detailed Substance Profile

Preferred Name
HYDROGENATED COTTONSEED OIL
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
Z82Y2C65EA
The specific atomic composition represented as a molecular structure string.
Substance Type
structurallyDiverse
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
ITIS TSN
21711
Taxonomic Serial Number for species identified in the Integrated Taxonomic Information System.
NCBI Taxonomy
3635
Unique numeric identifier used to specify biological species in the NCBI database.
USDA PLANTS ID
GOHI
Botanical identifier maintained by the U.S. Department of Agriculture.
GRIN Nomen ID
17917
Identifier from the Germplasm Resources Information Network botanical database.
MPNS Record
WCSCMP-2831092
Record ID from the Kew Royal Botanic Gardens Medicinal Plants Name Service.

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Hydrogenated Cottonseed Oil. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.

FDA Official Name

HYDROGENATED COTTONSEED OIL

Common Names & Synonyms

COTTONSEED OIL, HYDROGENATED
COTTONSEED OIL, HYDROGENATED [EP MONOGRAPH]
COTTONSEED OIL, HYDROGENATED [II]
HYDROGENATED COTTONSEED OIL [MART.]
HYDROGENATED COTTONSEED OIL [NF]

Brand / Trade Names

STEROTEX

NDC Products Containing HYDROGENATED COTTONSEED OIL

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 (446), only Active Listings are currently displayed. Display is limited to the first 200 products.
→ A-S Medication Solutions 22
→ Alembic Pharmaceuticals Inc. 3
→ Alembic Pharmaceuticals Limited 3
→ American Health Packaging 8
→ Amneal Pharmaceuticals LLC 3
→ Amneal Pharmaceuticals of New York LLC 5
→ Aurobindo Pharma Limited 25
→ AvKARE 6
→ AvPAK 7
→ BluePoint Laboratories 5
→ Bryant Ranch Prepack 8
→ Cardinal Health 107, LLC 7
→ Chartwell RX, LLC 2
→ Chattem, Inc. 1
→ Clinical Solutions Wholesale, LLC 2
→ Couper LLC 1
→ Coupler LLC 1
→ DirectRX 1
→ Dr. Reddy's Laboratories Limited 7
→ Dr. Reddys Laboratories Inc 3
→ Dr.Reddy's Laboratories Limited 1
→ EPIC PHARMA LLC 1
→ Epic Pharma, LLC 2
→ GenBioPro, Inc. 1
→ Golden State Medical Supply, Inc. 3
→ HF Acquisition Co LLC, DBA HealthFirst 1
→ Lil' Drug Store Products, Inc. 4
→ Macleods Pharmaceuticals Limited 2
→ Major Pharmaceuticals 6
→ Mayne Pharma 1
→ Mylan Institutional Inc. 2
→ NCS HealthCare of KY, LLC dba Vangard Labs 5
→ NorthStar Rx LLC 2
→ Northwind Health Company, LLC 4
→ NuCare Pharmaceuticals, Inc. 1
→ NuCare Pharmaceuticals,Inc. 1
→ PD-Rx Pharmaceuticals, Inc. 4
→ PML NYC, LLC 1
→ Proficient Rx LP 4
→ Redpharm Drug, inc. 1
→ Rising Pharma Holdings, Inc. 6
→ Safecor Health, LLC 2
→ Sandoz Inc 1
→ Strides Pharma Science Limited 3
→ Sun Pharmaceutical Industries, Inc. 1
→ Teva Pharmaceuticals USA, Inc. 10
→ Teva Women's Health LLC 3
→ Unichem Pharmaceuticals (USA), Inc. 3
→ Upsher-Smith Laboratories, LLC 4

A-S Medication Solutions

NDC Product
Human Prescription Drug

Cefuroxime Axetil
NDC 50090-0781

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

Cefuroxime Axetil
NDC 50090-0782

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

Junel Fe 28 Day
NDC 50090-3122

Generic Name
Norethindrone Acetate And Ethinyl Estradiol And Ferrous Fuma...
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Junel Fe 28 Day
NDC 50090-3237

Generic Name
Norethindrone Acetate And Ethinyl Estradiol And Ferrous Fuma...
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nitroglycerin
NDC 50090-3266

Generic Name
Nitroglycerin
Dosage Form
Tablet
Route
Sublingual
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Cefuroxime Axetil
NDC 50090-4153

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

Flecainide Acetate
NDC 50090-5306

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

Potassium Chloride
NDC 50090-5335

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

Cefuroxime Axetil
NDC 50090-6999

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

Metoprolol Succinate
NDC 50090-7069

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

Metoprolol Succinate
NDC 50090-7070

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

Cefuroxime Axetil
NDC 50090-7095

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

Metoprolol Succinate
NDC 50090-7117

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

Metoprolol Succinate
NDC 50090-7118

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

Metoprolol Succinate
NDC 50090-7238

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

Metoprolol Succinate
NDC 50090-7239

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

Potassium Chloride
NDC 50090-7378

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

Potassium Chloride
NDC 50090-7379

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

Potassium Chloride
NDC 50090-7639

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

Potassium Chloride
NDC 50090-7640

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

Cefuroxime Axetil
NDC 50090-7667

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

Cefuroxime Axetil
NDC 50090-7668

Generic Name
Cefuroxime Axetil
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Alembic Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Metronidazole
NDC 62332-016

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

Metronidazole
NDC 62332-017

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

Entacapone
NDC 62332-478

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

Alembic Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Metronidazole
NDC 46708-428

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

Metronidazole
NDC 46708-429

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

Entacapone
NDC 46708-478

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

American Health Packaging

NDC Product
Human Prescription Drug

Entacapone
NDC 60687-188

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

Metoprolol Succinate
NDC 60687-390

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

Metoprolol Succinate
NDC 60687-402

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

Metoprolol Succinate
NDC 60687-413

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

Misoprostol
NDC 60687-735

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

Misoprostol
NDC 60687-746

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

Chlordiazepoxide Hydrochloride
NDC 60687-807

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

Potassium Chloride
NDC 60687-810

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

Amneal Pharmaceuticals LLC

NDC Product
Human Prescription Drug

Oxybutynin Chloride
NDC 65162-371

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

Oxybutynin Chloride
NDC 65162-372

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

Oxybutynin Chloride
NDC 65162-373

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

Amneal Pharmaceuticals of New York LLC

NDC Product
Human Prescription Drug

Carvedilol Phosphate
NDC 0115-1248

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

Carvedilol Phosphate
NDC 0115-1249

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

Carvedilol Phosphate
NDC 0115-1250

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

Carvedilol Phosphate
NDC 0115-1251

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

Chloroquine Phosphate
NDC 0115-7010

Generic Name
Chloroquine Phosphate
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Aurobindo Pharma Limited

NDC Product
Human Prescription Drug

Silodosin
NDC 59651-095

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

Silodosin
NDC 59651-096

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

Zonisamide
NDC 59651-378

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

NDC 59651-378

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

NDC 59651-379

Generic Name
Zonisamide
Dosage Form
Capsule
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Zonisamide
NDC 59651-379

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

Zonisamide
NDC 59651-380

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

NDC 59651-380

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

NDC 65862-249

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

Alfuzosin Hydrochloride
NDC 65862-249

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

NDC 65862-621

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

Flecainide Acetate
NDC 65862-621

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

Flecainide Acetate
NDC 65862-622

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

NDC 65862-622

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

NDC 65862-623

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

Flecainide Acetate
NDC 65862-623

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

Entacapone
NDC 65862-654

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

Cefuroxime Axetil
NDC 65862-698

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

NDC 65862-698

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

NDC 65862-699

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

Cefuroxime Axetil
NDC 65862-699

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

Cefuroxime Axetil
NDC 65862-700

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

NDC 65862-700

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

Potassium Chloride
NDC 65862-986

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

Potassium Chloride
NDC 65862-987

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

AvKARE

NDC Product
Human Prescription Drug

Chloroquine Phosphate
NDC 42291-047

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

Carvedilol Phosphate
NDC 42291-479

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

Carvedilol Phosphate
NDC 42291-480

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

Carvedilol Phosphate
NDC 42291-481

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

Carvedilol Phosphate
NDC 42291-482

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

Potassium Chloride
NDC 42291-506

Generic Name
Potassium Chloride
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
NDA
Active Listing

AvPAK

NDC Product
Human Prescription Drug

Entacapone
NDC 50268-295

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

Metronidazole
NDC 50268-534

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

Metronidazole
NDC 50268-535

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

Metoprolol Succinate
NDC 50268-540

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 50268-541

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 50268-542

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 50268-543

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

BluePoint Laboratories

NDC Product
Human Prescription Drug

Levetiracetam
NDC 68001-113

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

Levetiracetam
NDC 68001-114

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

Metoprolol Succinate
NDC 68001-119

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

Metoprolol Succinate
NDC 68001-120

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

Potassium Chloride
NDC 68001-518

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

Bryant Ranch Prepack

NDC Product
Human Prescription Drug

Metronidazole
NDC 63629-1386

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

Bupropion Hydrochloride
NDC 63629-2138

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

Potassium Chloride
NDC 63629-2620

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

Chlordiazepoxide Hydrochloride
NDC 63629-3725

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

Junel Fe 28 Day
NDC 63629-5628

Generic Name
Norethindrone Acetate And Ethinyl Estradiol And Ferrous Fuma...
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Flecainide Acetate
NDC 63629-7979

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

Flecainide Acetate
NDC 63629-7982

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

Potassium Chloride Extended Release
NDC 63629-8442

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

Cardinal Health 107, LLC

NDC Product
Human Prescription Drug

Misoprostol
NDC 55154-2145

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

Metoprolol Succinate
NDC 55154-2642

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 55154-4347

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 55154-4698

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

Metoprolol Succinate
NDC 55154-6886

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 55154-7279

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 55154-7280

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

Chartwell RX, LLC

NDC Product
Human Prescription Drug

Carisoprodol
NDC 62135-241

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

Phentermine Hydrochloride
NDC 62135-959

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

Chattem, Inc.

NDC Product
Human Otc Drug

Dulcolax Laxative
NDC 41167-0222

Generic Name
Bisacodyl
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Clinical Solutions Wholesale, LLC

NDC Product
Human Prescription Drug

Chlordiazepoxide Hydrochloride
NDC 58118-1033

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

Chlordiazepoxide Hydrochloride
NDC 58118-1590

Generic Name
Chlordiazepoxide Hydrochloride
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

Couper LLC

NDC Product
Human Prescription Drug

Chlordiazepoxide Hydrochloride
NDC 67046-0910

Generic Name
Chlordiazepoxide Hydrochloride
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

Coupler LLC

NDC Product
Human Prescription Drug

Cefuroxime Axetil
NDC 67046-1307

Generic Name
Cefuroxime Axetil
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

DirectRX

Dr. Reddy's Laboratories Limited

NDC Product
Drug For Further Processing

NDC 55111-466

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

Metoprolol Succinate
NDC 55111-466

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 55111-467

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

NDC 55111-467

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

NDC 55111-468

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

Metoprolol Succinate
NDC 55111-468

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 55111-469

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

Dr. Reddys Laboratories Inc

NDC Product
Human Prescription Drug

Nitroglycerin
NDC 43598-435

Generic Name
Nitroglycerin
Dosage Form
Tablet
Route
Sublingual
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nitroglycerin
NDC 43598-436

Generic Name
Nitroglycerin
Dosage Form
Tablet
Route
Sublingual
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nitroglycerin
NDC 43598-437

Generic Name
Nitroglycerin
Dosage Form
Tablet
Route
Sublingual
Marketing
ANDA
Active Listing

Dr.Reddy's Laboratories Limited

NDC Product
Human Otc Drug

Fexofenadine Hcl And Pseudoephedrine Hci
NDC 55111-557

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

EPIC PHARMA LLC

NDC Product
Human Prescription Drug

Amantadine Hydrochloride
NDC 42806-716

Generic Name
Amantadine Hydrochloride
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

Epic Pharma, LLC

NDC Product
Human Prescription Drug

Potassium Chloride
NDC 42806-422

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

Potassium Chloride
NDC 42806-423

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

GenBioPro, Inc.

NDC Product
Human Prescription Drug

Misoprostol
NDC 43393-023

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

Golden State Medical Supply, Inc.

NDC Product
Human Prescription Drug

Nitroglycerin
NDC 60429-839

Generic Name
Nitroglycerin
Dosage Form
Tablet
Route
Sublingual
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nitroglycerin
NDC 60429-840

Generic Name
Nitroglycerin
Dosage Form
Tablet
Route
Sublingual
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Nitroglycerin
NDC 60429-841

Generic Name
Nitroglycerin
Dosage Form
Tablet
Route
Sublingual
Marketing
ANDA
Active Listing

HF Acquisition Co LLC, DBA HealthFirst

NDC Product
Human Prescription Drug

Nitroglycerin
NDC 51662-1282

Generic Name
Nitroglycerin
Dosage Form
Tablet
Route
Sublingual
Marketing
ANDA
Active Listing

Lil' Drug Store Products, Inc.

NDC Product
Human Otc Drug

Anti-diarrheal
NDC 29485-9286

Generic Name
Loperamide Hci
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Anti-diarrheal, Circle K
NDC 66715-5529

Generic Name
Loperamide Hcl Tablet
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Anti-diarrheal, Caseys 4good
NDC 66715-6359

Generic Name
Loperamide Hcl
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Anti-diarrheal, Cvp Health
NDC 66715-6559

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

Macleods Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Potassium Chloride
NDC 33342-417

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

Potassium Chloride
NDC 33342-418

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

Major Pharmaceuticals

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 0904-6322

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 0904-6323

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 0904-6324

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

Oxybutynin Chloride
NDC 0904-6570

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

Entacapone
NDC 0904-6822

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

Potassium Chloride
NDC 0904-7216

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

Mayne Pharma

NDC Product
Human Prescription Drug

Nextstellis
NDC 51862-258

Generic Name
Drospirenone And Estetrol
Dosage Form
Kit
Route
N/A
Marketing
NDA
Active Listing

Mylan Institutional Inc.

NDC Product
Human Prescription Drug

Chlordiazepoxide Hydrochloride
NDC 51079-141

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

Chlordiazepoxide Hydrochloride
NDC 51079-375

Generic Name
Chlordiazepoxide Hydrochloride
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

NCS HealthCare of KY, LLC dba Vangard Labs

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 0615-7823

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

Metoprolol Succinate
NDC 0615-7824

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

Metoprolol Succinate
NDC 0615-7825

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

Potassium Chloride
NDC 0615-8570

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

Potassium Chloride
NDC 0615-8580

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

NorthStar Rx LLC

NDC Product
Human Prescription Drug

Cefuroxime Axetil
NDC 16714-400

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

Cefuroxime Axetil
NDC 16714-401

Generic Name
Cefuroxime Axetil
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Northwind Health Company, LLC

NDC Product
Human Prescription Drug

Alfuzosin Hydrochloride
NDC 51655-087

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

Potassium Chloride
NDC 51655-226

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

Potassium Chloride
NDC 51655-463

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

Potassium Chloride
NDC 51655-706

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

NuCare Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Misoprostol
NDC 68071-3762

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

NuCare Pharmaceuticals,Inc.

NDC Product
Human Prescription Drug

Metronidazole
NDC 68071-2288

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

PD-Rx Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Chlordiazepoxide Hydrochloride
NDC 43063-046

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

Cefuroxime Axetil
NDC 43063-623

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

Metoprolol Succinate
NDC 43063-624

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 43063-841

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

PML NYC, LLC

Proficient Rx LP

NDC Product
Human Prescription Drug

Clopidogrel
NDC 63187-362

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

Metronidazole
NDC 63187-511

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

Metoprolol Succinate
NDC 63187-768

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

Junel Fe 1.5/30
NDC 63187-890

Generic Name
Norethindrone Acetate And Ethinyl Estradiol, And Ferrous Fum...
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing

Redpharm Drug, inc.

NDC Product
Human Prescription Drug

Metronidazole
NDC 67296-0078

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

Rising Pharma Holdings, Inc.

NDC Product
Human Prescription Drug

Cefuroxime Axetil
NDC 57237-058

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

Cefuroxime Axetil
NDC 57237-059

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

Flecainide Acetate
NDC 57237-063

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

Flecainide Acetate
NDC 57237-064

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

Flecainide Acetate
NDC 57237-065

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

Alfuzosin Hydrochloride
NDC 57237-114

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

Safecor Health, LLC

NDC Product
Human Prescription Drug

Chlordiazepoxide Hydrochloride
NDC 48433-019

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

Chlordiazepoxide Hydrochloride
NDC 48433-020

Generic Name
Chlordiazepoxide Hydrochloride
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

Sandoz Inc

NDC Product
Human Prescription Drug

Entacapone
NDC 0781-5578

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

Strides Pharma Science Limited

NDC Product
Human Prescription Drug

Potassium Chloride
NDC 64380-860

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

Potassium Chloride
NDC 64380-861

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

Amantadine Hydrochloride
NDC 64380-862

Generic Name
Amantadine Hydrochloride
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing

Sun Pharmaceutical Industries, Inc.

NDC Product
Human Prescription Drug

Entacapone
NDC 47335-007

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

Teva Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Junel Fe 24
NDC 0093-5328

Generic Name
Norethindrone Acetate And Ethinyl Estradiol And Ferrous Fuma...
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Clopidogrel
NDC 0093-7314

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

Chlordiazepoxide Hydrochloride
NDC 0555-0033

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

Chlordiazepoxide Hydrochloride
NDC 0555-0158

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

Chlordiazepoxide Hydrochloride
NDC 0555-0159

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

Junel Fe 28 Day
NDC 0555-9026

Generic Name
Norethindrone Acetate And Ethinyl Estradiol And Ferrous Fuma...
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Junel 21 Day
NDC 0555-9027

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

Junel Fe 28 Day
NDC 0555-9028

Generic Name
Norethindrone Acetate And Ethinyl Estradiol And Ferrous Fuma...
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Metronidazole
NDC 50111-333

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

Metronidazole
NDC 50111-334

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

Teva Women's Health LLC

NDC Product
Human Prescription Drug

Loestrin Fe 28 Day
NDC 51285-125

Generic Name
Norethindrone Acetate And Ethinyl Estradiol And Ferrous Fuma...
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Loestrin 21 Day
NDC 51285-127

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

Loestrin Fe 28 Day
NDC 51285-128

Generic Name
Norethindrone Acetate And Ethinyl Estradiol And Ferrous Fuma...
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing

Unichem Pharmaceuticals (USA), Inc.

NDC Product
Human Prescription Drug

Zonisamide
NDC 29300-428

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

Zonisamide
NDC 29300-429

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

Zonisamide
NDC 29300-430

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

Upsher-Smith Laboratories, LLC

NDC Product
Human Prescription Drug

Klor-con
NDC 0245-5315

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

Klor-con
NDC 0245-5316

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

Potassium Chloride
NDC 0832-5322

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

Potassium Chloride
NDC 0832-5323

Generic Name
Potassium Chloride
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
NDA
Active Listing

External Clinical & Regulatory Resources

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NCATS
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