ACETYLTRIBUTYL CITRATE
UNII 0ZBX0N59RZ

Substance Identification & Data

This profile provides standardized clinical and technical data for Acetyltributyl Citrate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 0ZBX0N59RZ.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 77-90-7 and the RxNorm Concept ID (RxCUI) 1362881. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
0ZBX0N59RZ
CAS Registry Number
77-90-7
RxNorm Concept ID
1362881

Detailed Substance Profile

Preferred Name
ACETYLTRIBUTYL CITRATE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
0ZBX0N59RZ
The specific atomic composition represented as a molecular structure string.
InChIKey
C20H34O8
International Chemical Identifier digital signature for unique molecular identification.
SMILES String
QZCLKYGREBVARF-UHFFFAOYSA-N
Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
C78760
National Cancer Institute reference terminology for clinical and research data.
PubChem CID
6505
Unique identification number in the NCBI database of chemical substances.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
C(CC(=O)OCCCC)(CC(=O)OCCCC)(C(=O)OCCCC)OC(=O)C

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Acetyltributyl Citrate. 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

ACETYL TRIBUTYL CITRATE

Common Names & Synonyms

1,2,3-PROPANETRICARBOXYLIC ACID, 2-(ACETYLOXY)-, 1,2,3-TRIBUTYL ESTER
2-ACETYLTRIBUTYLCITRATE
ACETYLTRIBUTYL CITRATE
ACETYLTRIBUTYL CITRATE [HSDB]
ACETYLTRIBUTYL CITRATE [II]
ACETYLTRIBUTYL CITRATE [USP-RS]
CITRIC ACID, O-ACETYLTRIBUTYL ESTER
TRIBUTYL ACETYLCITRATE [EP MONOGRAPH]
TRIBUTYL ACETYLCITRATE [FHFI]
TRIBUTYL ACETYLCITRATE [MART.]

Systematic Nomenclature

TRIBUTYL 2-ACETOXYPROPANE-1,2,3-TRICARBOXYLATE
TRIBUTYL ACETYLCITRATE

Technical Codes

FEMA NO. 3080
NSC-3894

NDC Products Containing ACETYLTRIBUTYL CITRATE

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 (326), only Active Listings are currently displayed. Display is limited to the first 200 products.
→ A-S Medication Solutions 15
→ Actavis Pharma, Inc. 12
→ Alembic Pharmaceuticals Inc. 5
→ Alembic Pharmaceuticals Limited 5
→ American Health Packaging 6
→ Amneal Pharmaceuticals of New York LLC 14
→ Aurobindo Pharma Limited 6
→ AvPAK 4
→ BluePoint Laboratories 5
→ Bryant Ranch Prepack 1
→ CHAIN DRUG MARKETING ASSOCIATION INC 1
→ Camber Pharmaceuticals, Inc. 4
→ Cardinal Health 107, LLC 6
→ Cipla USA Inc. 3
→ DirectRX 1
→ Discount Drug Mart, Inc 1
→ Dr. Reddy's Laboratories Inc 1
→ Dr. Reddy's Laboratories Inc. 1
→ Dr. Reddy's Laboratories Limited 7
→ Dr. Reddy�s Laboratories Inc. 1
→ Dr.Reddy's Laboratories Limited 1
→ Family Dollar (FAMILY WELLNESS) 1
→ Golden State Medical Supply, Inc. 1
→ Granules Pharmaceuticals Inc. 9
→ HEB 1
→ Lil' Drug Store Products, Inc. 1
→ Macleods Pharmaceuticals Limited 5
→ Major Pharmaceuticals 5
→ Mayne Pharma 2
→ NCS HealthCare of KY, LLC dba Vangard Labs 3
→ Northstar Rx LLC. 4
→ Northwind Health Company, LLC 3
→ NuCare Pharmaceutcals, Inc. 1
→ NuCare Pharmaceuticals,Inc. 2
→ P & L Development, LLC 3
→ PD-Rx Pharmaceuticals, Inc. 2
→ PLD Acquisitions LLC DBA Av�ma Pharma Solutions 4
→ Padagis US LLC 1
→ Preferred Pharmaceuticals Inc. 3
→ Proficient Rx LP 6
→ REMEDYREPACK INC. 9
→ Redpharm Drug 1
→ ST. MARY'S MEDICAL PARK PHARMACY 2
→ Smith & Nephew, Medical Ltd 1
→ Solventum US LLC 2
→ Sun Pharmaceutical Industries, Inc. 10
→ The Kroger Co. 1
→ Walgreens 1
→ Walgreens Company 1
→ WinCo Foods, LLC 1
→ Zydus Lifesciences Limited 7
→ Zydus Pharmaceuticals (USA) Inc. 5
→ Zydus Pharmaceuticals USA Inc. 2

A-S Medication Solutions

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 50090-6328

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

Metoprolol Succinate
NDC 50090-6662

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

Metoprolol Succinate
NDC 50090-6663

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

Glipizide
NDC 50090-6746

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

Glipizide
NDC 50090-6765

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

Glipizide
NDC 50090-6848

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

Glipizide
NDC 50090-6849

Generic Name
Glipizide
Dosage Form
Tablet, Extended Release
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

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

Metoprolol Succinate
NDC 50090-7590

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 50090-7591

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

Actavis Pharma, Inc.

NDC Product
Drug For Further Processing

NDC 45963-676

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

Metoprolol Succinate
NDC 45963-676

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 45963-677

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

NDC 45963-677

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

NDC 45963-678

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

Metoprolol Succinate
NDC 45963-678

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 45963-709

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

NDC 45963-709

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

Cartia Xt
NDC 62037-597

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

Cartia Xt
NDC 62037-598

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

Cartia Xt
NDC 62037-599

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

Cartia Xt
NDC 62037-600

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

Alembic Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 62332-725

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

Diltiazem Hydrochloride
NDC 62332-726

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

Diltiazem Hydrochloride
NDC 62332-727

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

Diltiazem Hydrochloride
NDC 62332-728

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

Diltiazem Hydrochloride
NDC 62332-729

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

Alembic Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 46708-725

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

Diltiazem Hydrochloride
NDC 46708-726

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

Diltiazem Hydrochloride
NDC 46708-727

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

Diltiazem Hydrochloride
NDC 46708-728

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

Diltiazem Hydrochloride
NDC 46708-729

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

American Health Packaging

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

Mesalamine
NDC 60687-408

Generic Name
Mesalamine
Dosage Form
Tablet, Delayed 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

Budesonide
NDC 60687-596

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

Glipizide
NDC 60687-768

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

Amneal Pharmaceuticals of New York LLC

NDC Product
Human Prescription Drug

Fenofibric Acid
NDC 0115-1324

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

Fenofibric Acid
NDC 0115-1325

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

Dexmethylphenidate Hydrochloride
NDC 0115-1682

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

Dexmethylphenidate Hydrochloride
NDC 0115-1683

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

Dexmethylphenidate Hydrochloride
NDC 0115-1684

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

Dexmethylphenidate Hydrochloride
NDC 0115-1685

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

Dexmethylphenidate Hydrochloride
NDC 0115-1686

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

Dexmethylphenidate Hydrochloride
NDC 0115-1709

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

Dexmethylphenidate Hydrochloride
NDC 0115-1710

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

Dexmethylphenidate Hydrochloride
NDC 0115-9918

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

Dexmethylphenidate Hydrochloride
NDC 0115-9919

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

Dexmethylphenidate Hydrochloride
NDC 0115-9920

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

Dexmethylphenidate Hydrochloride
NDC 0115-9921

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

Dexmethylphenidate Hydrochloride
NDC 0115-9922

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

Aurobindo Pharma Limited

NDC Product
Drug For Further Processing

NDC 59651-780

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

Glipizide
NDC 59651-780

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

Glipizide
NDC 59651-781

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

NDC 59651-781

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

NDC 59651-782

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

Glipizide
NDC 59651-782

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

AvPAK

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

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

Metoprolol Succinate
NDC 68001-469

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

Metoprolol Succinate
NDC 68001-470

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

Metoprolol Succinate
NDC 68001-471

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

Bryant Ranch Prepack

NDC Product
Human Prescription Drug

Cartia Xt
NDC 63629-7896

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

CHAIN DRUG MARKETING ASSOCIATION INC

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 63868-425

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

Camber Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 31722-589

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

Metoprolol Succinate
NDC 31722-590

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

Metoprolol Succinate
NDC 31722-591

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

Metoprolol Succinate
NDC 31722-592

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

Cardinal Health 107, LLC

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

Cipla USA Inc.

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 69097-407

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

Metoprolol Succinate
NDC 69097-408

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

Metoprolol Succinate
NDC 69097-409

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

DirectRX

Discount Drug Mart, Inc

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 53943-527

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

Dr. Reddy's Laboratories Inc

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 43598-407

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

Dr. Reddy's Laboratories Inc.

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 43598-812

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

Dr. Reddy's Laboratories Limited

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
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
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
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
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
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 55111-469

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

Dr. Reddy�s Laboratories Inc.

NDC Product
Drug For Further Processing

NDC 43598-407

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
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

Family Dollar (FAMILY WELLNESS)

NDC Product
Human Otc Drug

Omeprazole
NDC 55319-219

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

Golden State Medical Supply, Inc.

NDC Product
Human Prescription Drug

Budesonide
NDC 51407-591

Generic Name
Budesonide
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing

Granules Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Methylphenidate Hydrochloride
NDC 70010-012

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

Methylphenidate Hydrochloride
NDC 70010-013

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

Methylphenidate Hydrochloride
NDC 70010-014

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

Methylphenidate Hydrochloride
NDC 70010-015

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

Methylphenidate Hydrochloride
NDC 70010-016

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

Metoprolol Succinate
NDC 70010-780

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 70010-781

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 70010-782

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 70010-783

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

HEB

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 37808-115

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

Lil' Drug Store Products, Inc.

NDC Product
Human Otc Drug

Omeprazole, 24/7 Life By 7-eleven
NDC 66715-6550

Generic Name
Omeprazole Tablet, Delayed Release
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Macleods Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 33342-521

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

Diltiazem Hydrochloride
NDC 33342-522

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

Diltiazem Hydrochloride
NDC 33342-523

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

Diltiazem Hydrochloride
NDC 33342-524

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

Diltiazem Hydrochloride
NDC 33342-525

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

Major Pharmaceuticals

NDC Product
Human Prescription Drug

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

Mesalamine
NDC 0904-6832

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

Budesonide
NDC 0904-7313

Generic Name
Budesonide
Dosage Form
Capsule, Coated Pellets
Route
Oral
Marketing
ANDA
Active Listing

Mayne Pharma

NDC Product
Human Prescription Drug

Methylphenidate Hydrochloride (la)
NDC 51862-611

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

Methylphenidate Hydrochloride (la)
NDC 51862-612

Generic Name
Methylphenidate Hydrochloride
Dosage Form
Capsule, Extended Release
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

Northstar Rx LLC.

NDC Product
Human Prescription Drug

Budesonide
NDC 16714-829

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

Glipizide
NDC 16714-894

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

Glipizide
NDC 16714-895

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

Glipizide
NDC 16714-896

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

Northwind Health Company, LLC

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 51655-193

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 51655-519

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 51655-934

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

NuCare Pharmaceutcals, Inc.

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 68071-3828

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

NuCare Pharmaceuticals,Inc.

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 68071-3963

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 68071-5282

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

P & L Development, LLC

NDC Product
Human Otc Drug

Omeprazole
NDC 59726-298

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

Omeprazole
NDC 59726-740

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

Omeprazole
NDC 59726-744

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

PD-Rx Pharmaceuticals, Inc.

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

PLD Acquisitions LLC DBA Av�ma Pharma Solutions

NDC Product
Human Otc Drug

Omeprazole
NDC 63548-2970

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

Omeprazole
NDC 63548-4080

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

Omeprazole
NDC 63548-7370

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

Omeprazole
NDC 63548-8040

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

Padagis US LLC

NDC Product
Human Prescription Drug

Budesonide
NDC 0574-9855

Generic Name
Budesonide
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing

Preferred Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 68788-4022

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 68788-8312

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

Metoprolol Succinate
NDC 68788-8869

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

Proficient Rx LP

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

Metoprolol Succinate
NDC 71205-368

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 71205-683

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 71205-724

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 71205-800

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 71205-801

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

REMEDYREPACK INC.

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 70518-2080

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

Glipizide
NDC 70518-3645

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

Glipizide
NDC 70518-3896

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

Glipizide
NDC 70518-3898

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

Glipizide
NDC 70518-4128

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

Metoprolol Succinate
NDC 70518-4456

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 70518-4531

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 70518-4533

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

Budesonide
NDC 70518-4613

Generic Name
Budesonide
Dosage Form
Capsule, Coated Pellets
Route
Oral
Marketing
ANDA
Active Listing

Redpharm Drug

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 67296-2125

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

ST. MARY'S MEDICAL PARK PHARMACY

NDC Product
Human Prescription Drug

Glipizide
NDC 60760-793

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

Glipizide
NDC 60760-794

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

Smith & Nephew, Medical Ltd

NDC Product
Human Otc Drug

I.v. Prep Antiseptic Wipe
NDC 69740-212

Generic Name
Isopropyl Alcohol
Dosage Form
Cloth
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Solventum US LLC

NDC Product
Human Otc Drug

3m Soluprep S
NDC 17518-082

Generic Name
Chlorhexidine Gluconate And Isopropyl Alcohol
Dosage Form
Solution
Route
Topical
Marketing
NDA
Active Listing
NDC Product
Human Otc Drug

3m Soluprep S
NDC 17518-083

Generic Name
Chlorhexidine Gluconate And Isopropyl Alcohol
Dosage Form
Solution
Route
Topical
Marketing
NDA
Active Listing

Sun Pharmaceutical Industries, Inc.

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 47335-675

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

Diltiazem Hydrochloride
NDC 47335-676

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

Diltiazem Hydrochloride
NDC 47335-677

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

Diltiazem Hydrochloride
NDC 47335-678

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

Diltiazem Hydrochloride
NDC 47335-679

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

Diltiazem Hydrochloride
NDC 63304-718

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

Diltiazem Hydrochloride
NDC 63304-719

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

Diltiazem Hydrochloride
NDC 63304-720

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

Diltiazem Hydrochloride
NDC 63304-721

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

Diltiazem Hydrochloride
NDC 63304-722

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

The Kroger Co.

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 30142-261

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

Walgreens

NDC Product
Human Otc Drug

Omeprazole
NDC 0363-9510

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

Walgreens Company

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 0363-3298

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

WinCo Foods, LLC

NDC Product
Human Otc Drug

Omeprazole
NDC 67091-464

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

Zydus Lifesciences Limited

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 70771-1030

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

Diltiazem Hydrochloride
NDC 70771-1031

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

Diltiazem Hydrochloride
NDC 70771-1032

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

Diltiazem Hydrochloride
NDC 70771-1033

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

Diltiazem Hydrochloride
NDC 70771-1034

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

Budesonide
NDC 70771-1075

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

Mesalamine
NDC 70771-1110

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

Zydus Pharmaceuticals (USA) Inc.

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 68382-595

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

Diltiazem Hydrochloride
NDC 68382-596

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

Diltiazem Hydrochloride
NDC 68382-597

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

Diltiazem Hydrochloride
NDC 68382-598

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

Diltiazem Hydrochloride
NDC 68382-599

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

Zydus Pharmaceuticals USA Inc.

NDC Product
Human Prescription Drug

Mesalamine
NDC 68382-435

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

Budesonide
NDC 68382-720

Generic Name
Budesonide
Dosage Form
Capsule, Coated Pellets
Route
Oral
Marketing
ANDA
Active Listing

External Clinical & Regulatory Resources

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