METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)
UNII 74G4R6TH13

Substance Identification & Data

This profile provides standardized clinical and technical data for Methacrylic Acid - Methyl Methacrylate Copolymer (1:1), uniquely identified by the FDA Unique Ingredient Identifier (UNII) 74G4R6TH13.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 25086-15-1 and the RxNorm Concept ID (RxCUI) 1309720. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
74G4R6TH13
CAS Registry Number
25086-15-1
RxNorm Concept ID
1309720

Detailed Substance Profile

Preferred Name
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
74G4R6TH13
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
C80288
National Cancer Institute reference terminology for clinical and research data.
Substance Type
polymer
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Methacrylic Acid - Methyl Methacrylate Copolymer (1:1). Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.

Common Names & Synonyms

EUDRAGIT L 100
EUDRAGIT L 12.5
EUDRAGIT L 12.5 [II]
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) [EP IMPURITY]
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) [EP MONOGRAPH]
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) [II]
METHACRYLIC ACID AND METHYL METHACRYLATE COPOLYMER (1:1)
METHACRYLIC ACID AND METHYL METHACRYLATE COPOLYMER [USP-RS]
METHACRYLIC ACID COPOLYMER TYPE A
POLY(METHACRYLIC ACID, METHYL METHACRYLATE) (1:1)

Brand / Trade Names

EUDRAGIT L 12,5
EUDRAGIT L100

NDC Products Containing METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)

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 (500), only Active Listings are currently displayed. Display is limited to the first 200 products.
→ A-S Medication Solutions 25
→ AAA Pharmaceutical, Inc. 2
→ Accord Healthcare Inc. 2
→ Actavis Pharma, Inc. 8
→ Alembic Pharmaceuticals Limited 3
→ Aphena Pharma Solutions - Tennessee, LLC 2
→ AvKARE 2
→ AvPAK 5
→ BETTER LIVING BRANDS, LLC 1
→ Bayer HealthCare Pharmaceuticals Inc. 2
→ Camber Pharmaceuticals, Inc. 15
→ Cardinal Health 107, LLC 4
→ DISCOUNT DRUG MART 3
→ Dr. Reddy's Laboratories Inc. 2
→ Dr. Reddys Laboratories Limited 1
→ Endo USA, Inc. 1
→ GOODSENSE 1
→ Golden State Medical Supply, Inc. 15
→ HEB 1
→ HYVEE INC 1
→ Haleon US Holdings LLC 2
→ Ingenus Pharmaceuticals, LLC 4
→ Lannett Company Inc. 1
→ Macleods Pharmaceuticals Limited 3
→ Major Pharmaceuticals 3
→ Marlex Pharmaceuticals Inc. 1
→ Micro Labs Limited 3
→ Mylan Pharmaceuticals Inc. 3
→ NCS HealthCare of KY, LLC dba Vangard Labs 2
→ Nortec Development Associates, Inc. 6
→ NorthStar RxLLC 4
→ Northstar Rx LLC. 3
→ Northwind Health Company, LLC 6
→ PD-Rx Pharmaceuticals, Inc. 1
→ Par Health USA, LLC 10
→ Pfizer Laboratories Div Pfizer Inc 2
→ QPharma Inc 1
→ Revlon Consumer Products Corp 1
→ Safeway 2
→ Solco Healthcare US, LLC 2
→ Sun Pharmaceutical Industries, Inc. 4
→ TIME CAP LABORATORIES, INC. 1
→ Takeda Pharmaceuticals America, Inc. 12
→ Teva Pharmaceuticals USA, Inc. 12
→ Teva Pharmaceuticals, Inc. 1
→ TopCare 1
→ United Natural Foods, Inc. dba UNFI 1
→ Upsher-Smith Laboratories, LLC 11
→ WALGREENS 1

A-S Medication Solutions

NDC Product
Human Prescription Drug

Diclofenac Sodium Delayed Release
NDC 50090-0542

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

Diclofenac Sodium Delayed Release
NDC 50090-0543

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

Diclofenac Sodium Delayed Release
NDC 50090-0545

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

Nexium 24hr
NDC 50090-1492

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Dimethyl Fumarate
NDC 50090-5288

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

Pantoprazole Sodium
NDC 50090-5793

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

Pantoprazole Sodium
NDC 50090-5794

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

Dexlansoprazole Delayed Release
NDC 50090-5944

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

Nifedipine
NDC 50090-6201

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

Nifedipine
NDC 50090-6203

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

Nifedipine
NDC 50090-6450

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

Dexlansoprazole Delayed Release
NDC 50090-6514

Generic Name
Dexlansoprazole
Dosage Form
Capsule, Delayed 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 Otc Drug

Aspirin
NDC 50090-7623

Generic Name
Aspirin
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Aspirin
NDC 50090-7624

Generic Name
Aspirin
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription Drug

Diclofenac Sodium
NDC 50090-7646

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

Diclofenac Sodium
NDC 50090-7647

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

Diclofenac Sodium Delayed Release
NDC 50090-7818

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

Diclofenac Sodium Delayed Release
NDC 50090-7838

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

Diclofenac Sodium Delayed Release
NDC 50090-7839

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

Diclofenac Sodium Delayed Release
NDC 50090-7880

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

Diclofenac Sodium Delayed Release
NDC 50090-7881

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

AAA Pharmaceutical, Inc.

NDC Product
Human Otc Drug

Aspirin
NDC 57344-080

Generic Name
Aspirin
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Aspirin
NDC 57344-146

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

Accord Healthcare Inc.

NDC Product
Human Prescription Drug

Dimethyl Fumarate
NDC 16729-416

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

Dimethyl Fumarate
NDC 16729-417

Generic Name
Dimethyl Fumarate
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
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
NDC Product
Human Prescription Drug

Mesalamine
NDC 0591-2245

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

Budesonide
NDC 0591-2510

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

Alembic Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Mesalamine
NDC 46708-724

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

Dexlansoprazole
NDC 46708-823

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

Dexlansoprazole
NDC 46708-824

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

Aphena Pharma Solutions - Tennessee, LLC

NDC Product
Human Prescription Drug

Pantoprazole Sodium
NDC 43353-027

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

Omeprazole
NDC 43353-829

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

AvKARE

NDC Product
Human Prescription Drug

Dutasteride And Tamsulosin Hydrochloride
NDC 42291-031

Generic Name
Dutasteride And Tamsulosin Hydrochloride Capsules
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Mesalamine
NDC 42291-489

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

AvPAK

NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 50268-259

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

Divalproex Sodium
NDC 50268-260

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

Mesalamine
NDC 50268-577

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

Pantoprazole Sodium
NDC 50268-585

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

Pantoprazole Sodium
NDC 50268-639

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

BETTER LIVING BRANDS, LLC

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 21130-718

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

Bayer HealthCare Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Cipro
NDC 50419-773

Generic Name
Ciprofloxacin
Dosage Form
Kit
Route
N/A
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Cipro
NDC 50419-777

Generic Name
Ciprofloxacin
Dosage Form
Kit
Route
N/A
Marketing
NDA
Active Listing

Camber Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Mesalamine
NDC 31722-043

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

Dexmethylphenidate Hydrochloride
NDC 31722-229

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

Dexmethylphenidate Hydrochloride
NDC 31722-230

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

Dexmethylphenidate Hydrochloride
NDC 31722-231

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

Dexmethylphenidate Hydrochloride
NDC 31722-232

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

Dexmethylphenidate Hydrochloride
NDC 31722-233

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

Dexmethylphenidate Hydrochloride
NDC 31722-234

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

Dexmethylphenidate Hydrochloride
NDC 31722-235

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

Dexmethylphenidate Hydrochloride
NDC 31722-236

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

Mesalamine
NDC 31722-489

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

Dimethyl Fumarate
NDC 31722-657

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

Dimethyl Fumarate
NDC 31722-658

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

Dimethyl Fumarate
NDC 31722-680

Generic Name
Dimethyl Fumarate
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Pantoprazole Sodium
NDC 31722-712

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

Pantoprazole Sodium
NDC 31722-713

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

Cardinal Health 107, LLC

NDC Product
Human Prescription Drug

Divalproex Sodium
NDC 55154-2345

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

Nifedipine
NDC 55154-4157

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

Pantoprazole Sodium
NDC 55154-4346

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

Divalproex Sodium
NDC 55154-4759

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

DISCOUNT DRUG MART

NDC Product
Human Otc Drug

Low Dose Aspirin
NDC 53943-080

Generic Name
Aspirin
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Enteric Coated Aspirin
NDC 53943-081

Generic Name
Aspirin
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Adult Low Strength Aspirin
NDC 53943-146

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

Dr. Reddy's Laboratories Inc.

NDC Product
Human Prescription Drug

Dimethyl Fumarate
NDC 43598-429

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

Dimethyl Fumarate
NDC 43598-430

Generic Name
Dimethyl Fumarate
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Dr. Reddys Laboratories Limited

NDC Product
Human Prescription Drug

Donepezil Hydrochloride
NDC 55111-302

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

Endo USA, Inc.

GOODSENSE

NDC Product
Human Otc Drug

Aspirin
NDC 50804-880

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

Golden State Medical Supply, Inc.

NDC Product
Human Prescription Drug

Carvedilol Phosphate
NDC 51407-050

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

Carvedilol Phosphate
NDC 51407-051

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

Carvedilol Phosphate
NDC 51407-052

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

Carvedilol Phosphate
NDC 51407-053

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

Dimethyl Fumarate
NDC 51407-441

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

Diclofenac Sodium Delayed Release
NDC 51407-536

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

Diclofenac Sodium Delayed Release
NDC 51407-537

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

Diclofenac Sodium Delayed Release
NDC 51407-538

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

Pantoprazole Sodium
NDC 51407-612

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

Pantoprazole Sodium
NDC 51407-613

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

Dexlansoprazole Delayed Release
NDC 51407-746

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

Dexlansoprazole Delayed Release
NDC 51407-747

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

Diclofenac Sodium Delayed Release
NDC 51407-967

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

Diclofenac Sodium Delayed Release
NDC 51407-968

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

Mesalamine
NDC 51407-976

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

HEB

NDC Product
Human Otc Drug

Aspirin 81 Mg Low Dose
NDC 37808-246

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

HYVEE INC

NDC Product
Human Otc Drug

Aspirin 81 Mg
NDC 42507-080

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

Haleon US Holdings LLC

NDC Product
Human Otc Drug

Nexium 24hr
NDC 0573-2450

Generic Name
Esomeprazole Magnesium
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Otc Drug

Nexium 24hr Clearminis
NDC 0573-2452

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

Ingenus Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Nifedipine
NDC 50742-260

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

Nifedipine
NDC 50742-261

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

Nifedipine
NDC 50742-262

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

Mesalamine
NDC 50742-371

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

Lannett Company Inc.

NDC Product
Human Prescription Drug

Mesalamine
NDC 0527-3012

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

Macleods Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Dimethyl Fumarate
NDC 33342-349

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

Dimethyl Fumarate
NDC 33342-350

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

Dimethyl Fumarate
NDC 33342-351

Generic Name
Dimethyl Fumarate
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing

Major Pharmaceuticals

NDC Product
Human Prescription Drug

Nifedipine
NDC 0904-7081

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

Nifedipine
NDC 0904-7082

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

Divalproex Sodium
NDC 0904-7182

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

Marlex Pharmaceuticals Inc.

NDC Product
Human Otc Drug

Aspirin
NDC 10135-729

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

Micro Labs Limited

NDC Product
Human Prescription Drug

Aspirin And Extended-release Dipyridamole
NDC 42571-274

Generic Name
Aspirin And Extended-release Dipyridamole
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Metformin Hydrochloride
NDC 42571-333

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

Metformin Hydrochloride
NDC 42571-334

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

Mylan Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Mesalamine
NDC 0378-1375

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

Budesonide
NDC 0378-4500

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

Acamprosate Calcium
NDC 0378-6333

Generic Name
Acamprosate Calcium Enteric-coated
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

NCS HealthCare of KY, LLC dba Vangard Labs

NDC Product
Human Prescription Drug

Nifedipine
NDC 0615-8549

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

Acamprosate Calcium
NDC 0615-8560

Generic Name
Acamprosate Calcium Enteric-coated
Dosage Form
Tablet, Delayed Release
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 RxLLC

NDC Product
Human Prescription Drug

Carvedilol Phosphate
NDC 16714-227

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

Carvedilol Phosphate
NDC 16714-228

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

Carvedilol Phosphate
NDC 16714-229

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

Carvedilol Phosphate
NDC 16714-230

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

Northstar Rx LLC.

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

Diclofenac Sodium Delayed Release
NDC 51655-176

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

Diclofenac Sodium Delayed Release
NDC 51655-280

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

Nifedipine
NDC 51655-386

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

Nifedipine
NDC 51655-407

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

Nifedipine
NDC 51655-593

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

Pantoprazole Sodium
NDC 51655-744

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

PD-Rx Pharmaceuticals, Inc.

NDC Product
Human Otc Drug

Aspirin
NDC 43063-724

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

Par Health USA, LLC

NDC Product
Human Prescription Drug

Dexmethylphenidate Hydrochloride
NDC 49884-048

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

Dexmethylphenidate Hydrochloride
NDC 49884-049

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

Alprazolam
NDC 49884-110

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

Alprazolam
NDC 49884-111

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

Alprazolam
NDC 49884-213

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

Alprazolam
NDC 49884-214

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

Dexmethylphenidate Hydrochloride
NDC 49884-248

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

Dexmethylphenidate Hydrochloride
NDC 49884-333

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

Dexmethylphenidate Hydrochloride
NDC 49884-339

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

Dexmethylphenidate Hydrochloride
NDC 49884-546

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

Pfizer Laboratories Div Pfizer Inc

NDC Product
Human Prescription Drug

Arthrotec
NDC 0025-1411

Generic Name
Diclofenac Sodium And Misoprostol
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Arthrotec
NDC 0025-1421

Generic Name
Diclofenac Sodium And Misoprostol
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing

QPharma Inc

NDC Product
Human Prescription Drug

Pantoprazole Sodium
NDC 42708-104

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

Revlon Consumer Products Corp

NDC Product
Human Otc Drug

Revlon Photoready Insta-fix Makeup
NDC 10967-631

Generic Name
Titanium Dioxide, Zinc Oxide
Dosage Form
Stick
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Safeway

NDC Product
Human Otc Drug

Omeprazole
NDC 21130-528

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

Solco Healthcare US, LLC

NDC Product
Human Prescription Drug

Dimethyl Fumarate
NDC 43547-024

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

Dimethyl Fumarate
NDC 43547-025

Generic Name
Dimethyl Fumarate
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing

Sun Pharmaceutical Industries, Inc.

NDC Product
Human Prescription Drug

Carvedilol Phosphate
NDC 57664-663

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

Carvedilol Phosphate
NDC 57664-664

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

Carvedilol Phosphate
NDC 57664-665

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

Carvedilol Phosphate
NDC 57664-666

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

TIME CAP LABORATORIES, INC.

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 49483-718

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

Takeda Pharmaceuticals America, Inc.

NDC Product
Human Prescription Drug

Mesalamine
NDC 54092-100

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

Adderall Xr
NDC 54092-381

Generic Name
Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amp...
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Adderall Xr
NDC 54092-383

Generic Name
Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amp...
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Adderall Xr
NDC 54092-385

Generic Name
Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amp...
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Adderall Xr
NDC 54092-387

Generic Name
Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amp...
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Adderall Xr
NDC 54092-389

Generic Name
Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amp...
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Adderall Xr
NDC 54092-391

Generic Name
Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amp...
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Lialda
NDC 54092-476

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

Intuniv
NDC 54092-513

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

Intuniv
NDC 54092-515

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

Intuniv
NDC 54092-517

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

Intuniv
NDC 54092-519

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

Teva Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Dexmethylphenidate Hydrochloride
NDC 0093-5045

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

Dexmethylphenidate Hydrochloride
NDC 0093-5046

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

Methylphenidate Hydrochloride (la)
NDC 0093-5346

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

Methylphenidate Hydrochloride (la)
NDC 0093-5347

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

Methylphenidate Hydrochloride (la)
NDC 0093-5348

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

Dexmethylphenidate Hydrochloride
NDC 0093-5550

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

Dexmethylphenidate Hydrochloride
NDC 0093-5551

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

Dexmethylphenidate Hydrochloride
NDC 0093-5552

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

Dexmethylphenidate Hydrochloride
NDC 0093-5553

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

Dexmethylphenidate Hydrochloride
NDC 0093-5554

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

Dexmethylphenidate Hydrochloride
NDC 0093-5562

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

Mesalamine
NDC 0093-9224

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

Teva Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Mesalamine
NDC 0480-7750

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

TopCare

NDC Product
Human Otc Drug

Aspirin 81mg Adult Low Dose
NDC 36800-880

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

United Natural Foods, Inc. dba UNFI

NDC Product
Human Otc Drug

Aspirin Regular Strength
NDC 41163-522

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

Upsher-Smith Laboratories, LLC

NDC Product
Human Prescription Drug

Mesalamine
NDC 0832-6056

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

Dexlansoprazole Delayed Release
NDC 24979-001

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

Dexlansoprazole Delayed Release
NDC 24979-002

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

Dimethyl Fumarate
NDC 24979-127

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

Dimethyl Fumarate
NDC 24979-128

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

Naprelan
NDC 24979-249

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

Naprelan
NDC 24979-250

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

Naprelan
NDC 24979-251

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

Naproxen Sodium
NDC 24979-252

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

Naproxen Sodium
NDC 24979-253

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

Naproxen Sodium
NDC 24979-254

Generic Name
Naproxen Sodium
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing

WALGREENS

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