DIETHYL PHTHALATE
UNII UF064M00AF

Substance Identification & Data

This profile provides standardized clinical and technical data for Diethyl Phthalate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) UF064M00AF.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 84-66-2 and the RxNorm Concept ID (RxCUI) 1362921. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
UF064M00AF
CAS Registry Number
84-66-2
RxNorm Concept ID
1362921

Detailed Substance Profile

Preferred Name
DIETHYL PHTHALATE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
UF064M00AF
The specific atomic composition represented as a molecular structure string.
InChIKey
C12H14O4
International Chemical Identifier digital signature for unique molecular identification.
SMILES String
FLKPEMZONWLCSK-UHFFFAOYSA-N
Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
C76749
National Cancer Institute reference terminology for clinical and research data.
PubChem CID
6781
Unique identification number in the NCBI database of chemical substances.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
c1(c(C(=O)OCC)cccc1)C(=O)OCC

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Diethyl Phthalate. 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

DIETHYL PHTHALATE

Common Names & Synonyms

1,2-BENZENEDICARBOXYLIC ACID, DIETHYL ESTER
DIETHYL PHTHALATE [EP MONOGRAPH]
DIETHYL PHTHALATE [HSDB]
DIETHYL PHTHALATE [II]
DIETHYL PHTHALATE [MART.]
DIETHYL PHTHALATE [USP-RS]
DIETHYL PHTHALATE [VANDF]
ETHYL PHTHALATE [WHO-DD]
O-PHTHALIC ACID, DIETHYL ESTER
PHTHALIC ACID ETHYL ESTER [MI]

Systematic Nomenclature

ETHYL PHTHALATE
PHTHALIC ACID ETHYL ESTER

Technical Codes

NSC-8905

NDC Products Containing DIETHYL PHTHALATE

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 (287), only Active Listings are currently displayed. Display is limited to the first 200 products.
→ A-S Medication Solutions 2
→ ANI Pharmaceuticals, Inc. 4
→ Actavis Pharma, Inc. 6
→ Akron Pharma Inc. 1
→ American Health Packaging 6
→ Amneal Pharmaceuticals LLC 3
→ Amneal Pharmaceuticals of New York LLC 9
→ Aphena Pharma Solutions - Tennessee, LLC 1
→ Aurobindo Pharma Limited 3
→ AvKARE 6
→ Breckenridge Pharmaceutical, Inc. 4
→ Bryant Ranch Prepack 30
→ Cardinal Health 107, LLC 2
→ Cephalon, LLC 2
→ Coupler LLC 1
→ Coupler, LLC 1
→ Direct_Rx 3
→ Doc Rx 1
→ GLENMARK PHARMACEUTICALS INC., USA 4
→ Glenmark Pharmaceuticals Inc., USA 5
→ Golden State Medical Supply, Inc. 4
→ Ingenus Pharmaceuticals, LLC 8
→ Major Pharmaceuticals 4
→ Mylan Institutional Inc. 4
→ Mylan Pharmaceuticals Inc. 6
→ NCS HealthCare of KY, LLC dba Vangard Labs 7
→ Nortec Development Associates, Inc. 6
→ Northstar Rx LLC 3
→ NuCare Pharmaceuticals,Inc. 1
→ PD-Rx Pharmaceuticals, Inc. 2
→ Preferred Pharmaceuticals Inc. 3
→ Proficient Rx LP 1
→ REMEDYREPACK INC. 13
→ Rising Pharma Holdings, Inc. 3
→ ST. MARY'S MEDICAL PARK PHARMACY 3
→ Safecor Health LLC 3
→ Sun Pharmaceutical Industries, Inc. 8
→ Sunrise Pharmaceutical, Inc. 1
→ Teva Pharmaceuticals USA, Inc. 2
→ Torrent Pharmaceuticals Limited 7
→ Upsher-Smith Laboratories, LLC 17

A-S Medication Solutions

NDC Product
Human Prescription Drug

Propranolol Hydrochloride
NDC 50090-1501

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

Divalproex Sodium
NDC 50090-7121

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

ANI Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Innopran Xl
NDC 62559-590

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

Innopran Xl
NDC 62559-591

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

Inderal Xl
NDC 62559-600

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

Inderal Xl
NDC 62559-601

Generic Name
Propranolol Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA
Active Listing

Actavis Pharma, Inc.

NDC Product
Human Prescription Drug

Morphine Sulfate
NDC 0228-3090

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

Morphine Sulfate
NDC 0228-3091

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

Morphine Sulfate
NDC 0228-3092

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

Morphine Sulfate
NDC 0228-3093

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

Morphine Sulfate
NDC 0228-3116

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

Morphine Sulfate
NDC 0228-3117

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

Akron Pharma Inc.

NDC Product
Human Otc Drug

Low Dose Aspirin
NDC 71399-1014

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

American Health Packaging

NDC Product
Human Prescription Drug

Propranolol Hydrochloride
NDC 60687-215

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

Propranolol Hydrochloride
NDC 60687-226

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

Potassium Chloride Extended-release
NDC 60687-632

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

Isosorbide Mononitrate
NDC 60687-794

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

Divalproex Sodium
NDC 68084-776

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

Divalproex Sodium
NDC 68084-782

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

Amneal Pharmaceuticals LLC

NDC Product
Human Prescription Drug

Prasugrel
NDC 65162-001

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

Prasugrel
NDC 65162-002

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

Rabeprazole Sodium
NDC 65162-724

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

Amneal Pharmaceuticals of New York LLC

NDC Product
Human Prescription Drug

Morphine Sulfate
NDC 0115-1277

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

Morphine Sulfate
NDC 0115-1278

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

Morphine Sulfate
NDC 0115-1279

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

Morphine Sulfate
NDC 0115-1280

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

Morphine Sulfate
NDC 0115-1281

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

Morphine Sulfate
NDC 0115-1282

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

Cyclobenzaprine Hydrochloride
NDC 0115-1436

Generic Name
Cyclobenzaprine Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Cyclobenzaprine Hydrochloride
NDC 0115-1437

Generic Name
Cyclobenzaprine Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate
NDC 0115-1479

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

Aphena Pharma Solutions - Tennessee, LLC

NDC Product
Human Prescription Drug

Carbamazepine
NDC 71610-782

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

Aurobindo Pharma Limited

NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 65862-402

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

Divalproex Sodium
NDC 65862-403

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

Divalproex Sodium
NDC 65862-959

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

AvKARE

NDC Product
Human Prescription Drug

Propranolol Hydrochloride
NDC 42291-522

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

Propranolol Hydrochloride
NDC 42291-523

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

Propranolol Hydrochloride
NDC 42291-524

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

Propranolol Hydrochloride
NDC 42291-525

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

Breckenridge Pharmaceutical, Inc.

NDC Product
Human Prescription Drug

Propranolol Hydrochloride
NDC 51991-817

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

Propranolol Hydrochloride
NDC 51991-818

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

Propranolol Hydrochloride
NDC 51991-819

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

Propranolol Hydrochloride
NDC 51991-820

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

Bryant Ranch Prepack

NDC Product
Human Prescription Drug

Potassium Chloride Extended-release
NDC 63629-1072

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

Potassium Chloride Extended-release
NDC 63629-1073

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

Potassium Chloride Extended-release
NDC 63629-1074

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

Potassium Chloride Extended-release
NDC 63629-1075

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

Propranolol Hydrochloride
NDC 63629-2069

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

Propranolol Hydrochloride
NDC 63629-2070

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

Propranolol Hydrochloride
NDC 63629-2071

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

Propranolol Hydrochloride
NDC 63629-2072

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

Cyclobenzaprine Hydrochloride
NDC 63629-8206

Generic Name
Cyclobenzaprine Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Propranolol Hydrochloride
NDC 63629-9282

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

Propranolol Hydrochloride
NDC 71335-0234

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

Carbamazepine
NDC 71335-0461

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

Diltiazem Hydrochloride
NDC 71335-1776

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

Diltiazem Hydrochloride
NDC 71335-1897

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

Potassium Chloride Extended-release
NDC 71335-1900

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

Diltiazem Hydrochloride
NDC 71335-2089

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

Divalproex Sodium
NDC 71335-2158

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

Propranolol Hydrochloride
NDC 71335-2315

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

Diltiazem Hydrochloride
NDC 71335-2602

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

Potassium Chloride Extended-release
NDC 71335-2607

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

Cyclobenzaprine Hydrochloride
NDC 71335-2696

Generic Name
Cyclobenzaprine Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Propranolol Hydrochloride
NDC 71335-2781

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

Potassium Chloride Extended-release
NDC 71335-2866

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

Potassium Chloride Extended-release
NDC 71335-2913

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

Potassium Chloride Extended-release
NDC 71335-2958

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

Diltiazem Hydrochloride
NDC 71335-3091

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

Propranolol Hydrochloride
NDC 72162-1602

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

Propranolol Hydrochloride
NDC 72162-1604

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

Propranolol Hydrochloride
NDC 72162-1605

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

Potassium Chloride Extended-release
NDC 72162-1786

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

Cardinal Health 107, LLC

NDC Product
Human Prescription Drug

Isosorbide Mononitrate
NDC 55154-7291

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

Isosorbide Mononitrate
NDC 55154-7292

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

Cephalon, LLC

NDC Product
Human Prescription Drug

Amrix
NDC 63459-700

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

Amrix
NDC 63459-701

Generic Name
Cyclobenzaprine Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA
Active Listing

Coupler LLC

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 67046-1481

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

Coupler, LLC

NDC Product
Human Prescription Drug

Carbamazepine
NDC 67046-1534

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

Direct_Rx

NDC Product
Human Prescription Drug

Cyclobenzaprine Hcl Er
NDC 72189-362

Generic Name
Cyclobenzaprine Hcl Er
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Cyclobenzaprine Hcl Er
NDC 72189-389

Generic Name
Cyclobenzaprine Hcl Er
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Diltiazem Hcl Er
NDC 72189-409

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

Doc Rx

NDC Product
Human Prescription Drug

Cyclobenzaprine Hydrochloride
NDC 69306-015

Generic Name
Cyclobenzaprine Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing

GLENMARK PHARMACEUTICALS INC., USA

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 68462-562

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

Diltiazem Hydrochloride
NDC 68462-850

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

Diltiazem Hydrochloride
NDC 68462-851

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

Prochlorperazine Maleate
NDC 68462-889

Generic Name
Prochlorperazine Maleate
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Glenmark Pharmaceuticals Inc., USA

NDC Product
Human Prescription Drug

Chlorpromazine Hydrochloride
NDC 68462-861

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

Chlorpromazine Hydrochloride
NDC 68462-862

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

Chlorpromazine Hydrochloride
NDC 68462-863

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

Chlorpromazine Hydrochloride
NDC 68462-864

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

Chlorpromazine Hydrochloride
NDC 68462-865

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

Golden State Medical Supply, Inc.

NDC Product
Human Prescription Drug

Carbamazepine
NDC 51407-215

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

Carbamazepine
NDC 51407-895

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

Carbamazepine
NDC 51407-896

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

Carbamazepine
NDC 51407-897

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

Ingenus Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 50742-248

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

Diltiazem Hydrochloride
NDC 50742-249

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

Diltiazem Hydrochloride
NDC 50742-250

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

Diltiazem Hydrochloride
NDC 50742-251

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

Diltiazem Hydrochloride
NDC 50742-252

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

Diltiazem Hydrochloride
NDC 50742-564

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

Diltiazem Hydrochloride
NDC 50742-565

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

Diltiazem Hydrochloride
NDC 50742-566

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

Major Pharmaceuticals

NDC Product
Human Prescription Drug

Isosorbide Mononitrate
NDC 0904-6449

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

Isosorbide Mononitrate
NDC 0904-6450

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

Potassium Chloride Extended-release
NDC 0904-7547

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

Potassium Chloride
NDC 0904-7548

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

Mylan Institutional Inc.

NDC Product
Human Prescription Drug

Verapamil Hydrochloride
NDC 51079-917

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

Diltiazem Hydrochloride
NDC 51079-924

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

Diltiazem Hydrochloride
NDC 51079-925

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

Diltiazem Hydrochloride
NDC 51079-926

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

Mylan Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 0378-6060

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

Diltiazem Hydrochloride
NDC 0378-6090

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

Diltiazem Hydrochloride
NDC 0378-6120

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

Verapamil Hydrochloride
NDC 0378-6320

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

Verapamil Hydrochloride
NDC 0378-6380

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

Verapamil Hydrochloride
NDC 0378-6440

Generic Name
Verapamil 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

Isosorbide Mononitrate
NDC 0615-7767

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

Isosorbide Mononitrate
NDC 0615-7768

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

Carbamazepine
NDC 0615-8125

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

Diltiazem Hydrochloride
NDC 0615-8379

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

Diltiazem Hydrochloride
NDC 0615-8380

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

Diltiazem Hydrochloride
NDC 0615-8381

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

Carbamazepine
NDC 0615-8545

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

Nortec Development Associates, Inc.

NDC Product
Human Prescription Drug

Morphine Sulfate
NDC 42689-005

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

Morphine Sulfate
NDC 42689-006

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

Morphine Sulfate
NDC 42689-007

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

Morphine Sulfate
NDC 42689-008

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

Morphine Sulfate
NDC 42689-009

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

Morphine Sulfate
NDC 42689-010

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

Northstar Rx LLC

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 16714-553

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

Diltiazem Hydrochloride
NDC 16714-554

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

Diltiazem Hydrochloride
NDC 16714-555

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

NuCare Pharmaceuticals,Inc.

NDC Product
Human Prescription Drug

Carbamazepine
NDC 68071-2701

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

PD-Rx Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Carbamazepine
NDC 43063-328

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

Potassium Chloride
NDC 72789-365

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

Preferred Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Rabeprazole Sodium
NDC 68788-4060

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

Cyclobenzaprine Hydrochloride
NDC 68788-4087

Generic Name
Cyclobenzaprine Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 68788-7870

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

Proficient Rx LP

NDC Product
Human Prescription Drug

Rabeprazole Sodium
NDC 63187-555

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

REMEDYREPACK INC.

NDC Product
Human Prescription Drug

Lamotrigine
NDC 70518-1153

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

Carbamazepine
NDC 70518-1433

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

Propranolol Hydrochloride
NDC 70518-1463

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

Carbamazepine
NDC 70518-2242

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

Divalproex Sodium
NDC 70518-2357

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

Carbamazepine
NDC 70518-2426

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

Isosorbide Mononitrate
NDC 70518-2956

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

Potassium Chloride Extended-release
NDC 70518-3024

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

Divalproex Sodium
NDC 70518-3055

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

Diltiazem Hydrochloride
NDC 70518-3484

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

Divalproex Sodium
NDC 70518-3683

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

Cyclobenzaprine Hydrochloride
NDC 70518-4174

Generic Name
Cyclobenzaprine Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Cyclobenzaprine Hydrochloride
NDC 70518-4246

Generic Name
Cyclobenzaprine Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing

Rising Pharma Holdings, Inc.

NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 57237-047

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

Divalproex Sodium
NDC 57237-048

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

Divalproex Sodium
NDC 57237-106

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

ST. MARY'S MEDICAL PARK PHARMACY

NDC Product
Human Prescription Drug

Propranolol Hydrochloride
NDC 60760-589

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

Divalproex Sodium
NDC 60760-698

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

Propranolol Hydrochloride
NDC 60760-867

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

Safecor Health LLC

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 48433-030

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

Diltiazem Hydrochloride
NDC 48433-031

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

Diltiazem Hydrochloride
NDC 48433-032

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

Sun Pharmaceutical Industries, Inc.

NDC Product
Human Prescription Drug

Carbamazepine
NDC 51672-4005

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

Carbamazepine
NDC 51672-4041

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

Carbamazepine
NDC 51672-4047

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

Carbamazepine
NDC 51672-4123

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

Carbamazepine
NDC 51672-4124

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

Carbamazepine
NDC 51672-4125

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

Potassium Chloride Extended-release
NDC 63304-076

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

Potassium Chloride
NDC 63304-987

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

Sunrise Pharmaceutical, Inc.

NDC Product
Human Prescription Drug

Sulfasalazine
NDC 11534-201

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

Teva Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Cyclobenzaprine Hydrochloride
NDC 0093-1920

Generic Name
Cyclobenzaprine Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Cyclobenzaprine Hydrochloride
NDC 0093-1921

Generic Name
Cyclobenzaprine Hydrochloride
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing

Torrent Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Isosorbide Mononitrate
NDC 13668-104

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

Isosorbide Mononitrate
NDC 13668-105

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

Isosorbide Mononitrate
NDC 13668-106

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

Rabeprazole Sodium
NDC 13668-107

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

Lamotrigine
NDC 13668-339

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

Lamotrigine
NDC 13668-340

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

Lamotrigine
NDC 13668-341

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

Upsher-Smith Laboratories, LLC

NDC Product
Human Prescription Drug

Qudexy Xr
NDC 0245-1071

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

Qudexy Xr
NDC 0245-1072

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

Qudexy Xr
NDC 0245-1073

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

Qudexy Xr
NDC 0245-1074

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

Qudexy Xr
NDC 0245-1075

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

Morphine Sulfate
NDC 0832-0225

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

Morphine Sulfate
NDC 0832-0226

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

Morphine Sulfate
NDC 0832-0227

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

Morphine Sulfate
NDC 0832-0228

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

Morphine Sulfate
NDC 0832-0229

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

Morphine Sulfate
NDC 0832-0230

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

Morphine Sulfate
NDC 0832-0233

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

Topiramate
NDC 0832-1071

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

Topiramate
NDC 0832-1072

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

Topiramate
NDC 0832-1073

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

Topiramate
NDC 0832-1074

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

Topiramate
NDC 0832-1075

Generic Name
Topiramate
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing

External Clinical & Regulatory Resources

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