POVIDONE K30
UNII U725QWY32X

Substance Identification & Data

This profile provides standardized clinical and technical data for Povidone K30, uniquely identified by the FDA Unique Ingredient Identifier (UNII) U725QWY32X.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9003-39-8 and the RxNorm Concept ID (RxCUI) 1297406. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
U725QWY32X
CAS Registry Number
9003-39-8
RxNorm Concept ID
1297406

Detailed Substance Profile

Preferred Name
POVIDONE K30
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
U725QWY32X
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
C82262
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 Povidone K30. 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

390RMW2PEQ
POLYVINYLPYRROLIDONE K 30
POLYVINYLPYRROLIDONE K-29/32
POLYVINYLPYRROLIDONE K30
POVIDONE IMPURITY A [EP IMPURITY]
POVIDONE K29/32
POVIDONE K29/32 [II]
POVIDONE K29-32
POVIDONE K30
POVIDONE K30 [II]
PVP K30
PVP K-30
PVP-K 30

Brand / Trade Names

KOLLIDON 30
KOLLIDON 30 LP
PLASDONE C30
PLASDONE C-30
PLASDONE K29/32
PLASDONE K29-32

Systematic Nomenclature

1-ETHENYLPYRROLIDIN-2-ONE
1-VINYLPYRROLIDIN-2-ONE HOMOPOLYMER
2-PYRROLIDINONE, 1-ETHENYL-, HOMOPOLYMER

NDC Products Containing POVIDONE K30

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.
→ Actavis Pharma, Inc. 11
→ Amneal Pharmaceuticals of New York LLC 1
→ Bausch Health US LLC 6
→ Bayer HealthCare LLC. 2
→ Endo USA, Inc. 1
→ Genentech, Inc. 3
→ GlaxoSmithKline LLC 2
→ Hikma Pharmaceuticals USA Inc 1
→ Hikma Pharmaceuticals USA Inc. 19
→ Lannett Company, Inc. 4
→ Merck Sharp & Dohme LLC 5
→ Misemer Pharmaceuticals, Inc. 1
→ Mission Pharmacal Company 1
→ Mylan Pharmaceuticals Inc. 3
→ NCS HealthCare of KY, Inc dba Vangard Labs 3
→ NCS HealthCare of KY, LLC dba Vangard Labs 1
→ Novartis Pharmaceuticals Corporation 11
→ PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma 4
→ Padagis US LLC 6
→ Pfizer Laboratories Div Pfizer Inc 2
→ Rugby Laboratories 5
→ Teva Pharmaceuticals USA, Inc. 56
→ Teva Pharmaceuticals, Inc. 27
→ WALGREEN CO. 1
→ WALGREENS 6
→ WALGREENS CO. 2
→ Walgreen Company 1
→ Walgreens 12
→ Walgreens Company 2
→ walgreens 1

Actavis Pharma, Inc.

NDC Product
Human Prescription Drug

Propranolol Hydrochloride
NDC 0228-2778

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

Propranolol Hydrochloride
NDC 0228-2779

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

Propranolol Hydrochloride
NDC 0228-2780

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

Propranolol Hydrochloride
NDC 0228-2781

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

Buprenorphine
NDC 0228-3153

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

Buprenorphine And Naloxone
NDC 0228-3154

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

Buprenorphine And Naloxone
NDC 0228-3155

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

Buprenorphine
NDC 0228-3156

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

Diclofenac Sodium And Misoprostol
NDC 0591-0397

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

Diclofenac Sodium And Misoprostol
NDC 0591-0398

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

Bexarotene
NDC 0591-2832

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

Amneal Pharmaceuticals of New York LLC

NDC Product
Human Prescription Drug

Metaxalone
NDC 0115-1745

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

Bausch Health US LLC

NDC Product
Human Prescription Drug

Cardizem Cd
NDC 0187-0795

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

Cardizem Cd
NDC 0187-0796

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

Cardizem Cd
NDC 0187-0797

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

Cardizem Cd
NDC 0187-0798

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

Cardizem Cd
NDC 0187-0799

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

Tasmar
NDC 0187-0938

Generic Name
Tolcapone
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing

Bayer HealthCare LLC.

NDC Product
Human Otc Drug

Aleve
NDC 0280-6080

Generic Name
Naproxen Sodium
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Otc Drug

Aleve Easy Open Arthritis Cap
NDC 0280-6091

Generic Name
Naproxen Sodium
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
NDA
Active Listing

Endo USA, Inc.

NDC Product
Human Prescription Drug

Penicillamine
NDC 0254-2000

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

Genentech, Inc.

NDC Product
Human Prescription Drug

Tamiflu
NDC 0004-0800

Generic Name
Oseltamivir Phosphate
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Tamiflu
NDC 0004-0802

Generic Name
Oseltamivir Phosphate
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Tamiflu
NDC 0004-0822

Generic Name
Oseltamivir Phosphate
Dosage Form
Powder, For Suspension
Route
Oral
Marketing
NDA
Active Listing

GlaxoSmithKline LLC

NDC Product
Human Prescription Drug

Malarone
NDC 0173-0675

Generic Name
Atovaquone And Proguanil Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Malarone
NDC 0173-0676

Generic Name
Atovaquone And Proguanil Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing

Hikma Pharmaceuticals USA Inc

NDC Product
Human Prescription Drug

Combogesic
NDC 0143-9432

Generic Name
Acetaminophen And Ibuprofen
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing

Hikma Pharmaceuticals USA Inc.

NDC Product
Human Prescription Drug

Quetiapine Fumarate
NDC 0054-0220

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

Quetiapine Fumarate
NDC 0054-0221

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

Quetiapine Fumarate
NDC 0054-0222

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

Quetiapine Fumarate
NDC 0054-0223

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

Quetiapine Fumarate
NDC 0054-0229

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

Quetiapine Fumarate
NDC 0054-0230

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

Desvenlafaxine
NDC 0054-0400

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

Desvenlafaxine
NDC 0054-0401

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

Desvenlafaxine
NDC 0054-0603

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

Aminocaproic Acid
NDC 0054-1100

Generic Name
Aminocaproic Acid
Dosage Form
Syrup
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Aminocaproic Acid
NDC 0054-1110

Generic Name
Aminocaproic Acid
Dosage Form
Tablet
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Lithium Carbonate
NDC 0054-2526

Generic Name
Lithium Carbonate
Dosage Form
Capsule, Gelatin Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Lithium Carbonate
NDC 0054-2527

Generic Name
Lithium Carbonate
Dosage Form
Capsule, Gelatin Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Lithium Carbonate
NDC 0054-2531

Generic Name
Lithium Carbonate
Dosage Form
Capsule, Gelatin Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Meperidine Hydrochloride
NDC 0054-3545

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

Lithium Carbonate
NDC 0054-4527

Generic Name
Lithium Carbonate
Dosage Form
Tablet
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Lithium Carbonate
NDC 0054-8526

Generic Name
Lithium Carbonate
Dosage Form
Capsule, Gelatin Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Lithium Carbonate
NDC 0054-8527

Generic Name
Lithium Carbonate
Dosage Form
Capsule, Gelatin Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Lithium Carbonate
NDC 0054-8528

Generic Name
Lithium Carbonate
Dosage Form
Tablet
Route
Oral
Marketing
NDA
Active Listing

Lannett Company, Inc.

NDC Product
Human Prescription Drug

Diethylpropion Hydrochloride Er
NDC 0527-1477

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

Oseltamivir Phosphate
NDC 0527-4591

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

Oseltamivir Phosphate
NDC 0527-4592

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

Oseltamivir Phosphate
NDC 0527-4593

Generic Name
Oseltamivir Phosphate
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

Merck Sharp & Dohme LLC

NDC Product
Human Prescription Drug

Janumet Xr
NDC 0006-0078

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

Janumet Xr
NDC 0006-0080

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

Janumet Xr
NDC 0006-0081

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

Janumet
NDC 0006-0575

Generic Name
Sitagliptin And Metformin Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Janumet
NDC 0006-0577

Generic Name
Sitagliptin And Metformin Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing

Misemer Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Ketoprofen
NDC 0276-0504

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

Mission Pharmacal Company

NDC Product
Human Prescription Drug

Citranatal Assure
NDC 0178-0891

Generic Name
Ascorbic Acid, Calcium Citrate, Iron, Vitamin D, Dl- Alpha- ...
Dosage Form
Kit
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Mylan Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Scopolamine
NDC 0378-6470

Generic Name
Scopolamine
Dosage Form
Patch
Route
Transdermal
Marketing
ANDA
Active Listing

NCS HealthCare of KY, Inc dba Vangard Labs

NDC Product
Human Prescription Drug

Glimepiride
NDC 0615-8332

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

Glimepiride
NDC 0615-8333

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

Glimepiride
NDC 0615-8334

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

NCS HealthCare of KY, LLC dba Vangard Labs

NDC Product
Human Prescription Drug

Amiodarone Hydrochloride
NDC 0615-8258

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

Novartis Pharmaceuticals Corporation

NDC Product
Human Prescription Drug

Myfortic
NDC 0078-0385

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

Myfortic
NDC 0078-0386

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

Exjade
NDC 0078-0468

Generic Name
Deferasirox
Dosage Form
Tablet, For Suspension
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Exjade
NDC 0078-0469

Generic Name
Deferasirox
Dosage Form
Tablet, For Suspension
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Exjade
NDC 0078-0470

Generic Name
Deferasirox
Dosage Form
Tablet, For Suspension
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Jadenu
NDC 0078-0654

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

Jadenu
NDC 0078-0655

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

Jadenu
NDC 0078-0656

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

Jadenu
NDC 0078-0713

Generic Name
Deferasirox
Dosage Form
Granule
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Jadenu
NDC 0078-0720

Generic Name
Deferasirox
Dosage Form
Granule
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Jadenu
NDC 0078-0727

Generic Name
Deferasirox
Dosage Form
Granule
Route
Oral
Marketing
NDA
Active Listing

PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma

NDC Product
Human Prescription Drug

Buprenorphine And Naloxone
NDC 0121-1018

Generic Name
Buprenorphine Hydrochloride And Naloxone Hydrochloride
Dosage Form
Tablet
Route
Sublingual
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Buprenorphine Hydrochloride
NDC 0121-1019

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

Buprenorphine And Naloxone
NDC 0121-2036

Generic Name
Buprenorphine Hydrochloride And Naloxone Hydrochloride
Dosage Form
Tablet
Route
Sublingual
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Buprenorphine Hydrochloride
NDC 0121-2038

Generic Name
Buprenorphine Hydrochloride
Dosage Form
Tablet
Route
Sublingual
Marketing
ANDA
Active Listing

Padagis US LLC

NDC Product
Human Prescription Drug

Hydromorphone Hydrochloride
NDC 0574-0293

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

Hydromorphone Hydrochloride
NDC 0574-0294

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

Hydromorphone Hydrochloride
NDC 0574-0295

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

Hydromorphone Hydrochloride
NDC 0574-0297

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

Loteprednol Etabonate
NDC 0574-4080

Generic Name
Loteprednol Etabonate
Dosage Form
Suspension/ Drops
Route
Ophthalmic
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Loteprednol Etabonate
NDC 0574-4135

Generic Name
Loteprednol Etabonate
Dosage Form
Suspension/ Drops
Route
Ophthalmic
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

Rugby Laboratories

NDC Product
Human Otc Drug

Acetaminophen
NDC 0536-1172

Generic Name
Acetaminophen
Dosage Form
Tablet
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Mucus Relief Er
NDC 0536-1249

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

Olopatadine Hydrochloride
NDC 0536-1307

Generic Name
Olopatadine Hydrochloride
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Acetaminophen, Aspirin, Caffeine
NDC 0536-1326

Generic Name
Acetaminophen, Aspirin, Caffeine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Olopatadine Hcl
NDC 0536-1478

Generic Name
Olopatadine Hydrochloride
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
ANDA
Active Listing

Teva Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Carvedilol
NDC 0093-0051

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

Carvedilol
NDC 0093-0135

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

Atenolol
NDC 0093-0752

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

Atenolol
NDC 0093-0753

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

Piroxicam
NDC 0093-0756

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

Piroxicam
NDC 0093-0757

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

Atenolol
NDC 0093-0787

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

Diclofenac Potassium
NDC 0093-0948

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

Nefazodone Hydrochloride
NDC 0093-1024

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

Nefazodone Hydrochloride
NDC 0093-1025

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

Nefazodone Hydrochloride
NDC 0093-1026

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

Sotalol Hydrochloride
NDC 0093-1060

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

Sotalol Hydrochloride
NDC 0093-1061

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

Sotalol Hydrochloride
NDC 0093-1062

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

Sotalol Hydrochloride
NDC 0093-1063

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

Neomycin Sulfate
NDC 0093-1177

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

Cilostazol
NDC 0093-2064

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

Cilostazol
NDC 0093-2065

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

Reclipsen 28 Day
NDC 0093-3304

Generic Name
Desogestrel And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Almotriptan Malate
NDC 0093-5260

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

Almotriptan Malate
NDC 0093-5261

Generic Name
Almotriptan Malate
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0093-5571

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

Erythromycin
NDC 0093-5571

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

NDC 0093-5572

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

Erythromycin
NDC 0093-5572

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

Mesalamine
NDC 0093-5907

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

Nefazodone Hydrochloride
NDC 0093-7113

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

Nefazodone Hydrochloride
NDC 0093-7178

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

Raloxifene Hydrochloride
NDC 0093-7290

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

Carvedilol
NDC 0093-7295

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

Carvedilol
NDC 0093-7296

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

Mycophenolate Mofetil
NDC 0093-7334

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

Venlafaxine Hydrochloride
NDC 0093-7384

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

Venlafaxine Hydrochloride
NDC 0093-7385

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

Venlafaxine Hydrochloride
NDC 0093-7386

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

Glipizide And Metformin Hydrochloride
NDC 0093-7455

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

Glipizide And Metformin Hydrochloride
NDC 0093-7456

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

Glipizide And Metformin Hydrochloride
NDC 0093-7457

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

Anastrozole
NDC 0093-7536

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

Sunitinib Malate
NDC 0093-8199

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

Finzala
NDC 0093-8210

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

Sunitinib Malate
NDC 0093-8224

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

Sunitinib Malate
NDC 0093-8229

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

Sunitinib Malate
NDC 0093-8231

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

Irbesartan And Hydrochlorothiazide
NDC 0093-8232

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

Irbesartan And Hydrochlorothiazide
NDC 0093-8238

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

Balziva
NDC 0555-9034

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

Apri 28 Day
NDC 0555-9043

Generic Name
Desogestrel And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Kariva
NDC 0555-9050

Generic Name
Desogestrel/ethinyl Estradiol And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Velivet Triphasic Regimen
NDC 0555-9051

Generic Name
Desogestrel And Ethinyl Estradiol
Dosage Form
Kit
Route
N/A
Marketing
ANDA
Active Listing

Teva Pharmaceuticals, Inc.

NDC Product
Drug For Further Processing

NDC 0480-2299

Generic Name
Phentermine And Topiramate
Dosage Form
Capsule, Extended Release
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Phentermine And Topiramate
NDC 0480-2299

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

Lapatinib
NDC 0480-3237

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

Phentermine And Topiramate
NDC 0480-3295

Generic Name
Phentermine And Topiramate
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0480-3295

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

NDC 0480-3296

Generic Name
Phentermine And Topiramate
Dosage Form
Capsule, Extended Release
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Phentermine And Topiramate
NDC 0480-3296

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

Phentermine And Topiramate
NDC 0480-3297

Generic Name
Phentermine And Topiramate
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0480-3297

Generic Name
Phentermine And Topiramate
Dosage Form
Capsule, Extended Release
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Amethyst
NDC 0480-3472

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

Pitavastatin
NDC 0480-3631

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

Pitavastatin
NDC 0480-3632

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

Pitavastatin
NDC 0480-3633

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

Pazopanib
NDC 0480-4184

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

Deferasirox
NDC 0480-7011

Generic Name
Deferasirox
Dosage Form
Tablet, For Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Deferasirox
NDC 0480-7012

Generic Name
Deferasirox
Dosage Form
Tablet, For Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Deferasirox
NDC 0480-7013

Generic Name
Deferasirox
Dosage Form
Tablet, For Suspension
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Perampanel
NDC 0480-7062

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

Perampanel
NDC 0480-7063

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

Perampanel
NDC 0480-7065

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

Perampanel
NDC 0480-7066

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

Perampanel
NDC 0480-7067

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

Perampanel
NDC 0480-7068

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

Pravastatin Sodium
NDC 0480-7270

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

Mesalamine
NDC 0480-7750

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

NDC 0480-9242

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

Propylthiouracil
NDC 0480-9242

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

WALGREEN CO.

NDC Product
Human Otc Drug

Pain Reliever
NDC 0363-9947

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

WALGREENS

NDC Product
Human Otc Drug

Tension Headache Relief
NDC 0363-7213

Generic Name
Acetaminophen And Caffeine
Dosage Form
Tablet
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Extra Strength Headache Relief
NDC 0363-7214

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

Extra Strength Headache Relief
NDC 0363-8992

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

Acetaminophen
NDC 0363-9538

Generic Name
Acetaminophen
Dosage Form
Tablet
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Arthritis Pain Reliever
NDC 0363-9781

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

Acetaminophen
NDC 0363-9992

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

WALGREENS CO.

NDC Product
Human Otc Drug

Pamabrom
NDC 0363-0795

Generic Name
Pamabrom
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc Drug

Acetaminophen
NDC 0363-9993

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

Walgreen Company

NDC Product
Human Otc Drug

Eye Allergy Itch Relief
NDC 0363-1325

Generic Name
Olopatadine Hydrochloride Ophthalmic
Dosage Form
Solution
Route
Ophthalmic
Marketing
ANDA
Active Listing

Walgreens

NDC Product
Human Otc Drug

Pain Reliever Pm Extra Strength
NDC 0363-0863

Generic Name
Acetaminophen, Diphenhydramine Hcl
Dosage Form
Tablet, Coated
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Walgreens Effervescent Cold Relief Plus
NDC 0363-0875

Generic Name
Aspirin, Chlorpheniramine Maleate, Phenylephrine Bitartrate
Dosage Form
Tablet, Effervescent
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Acetaminophen
NDC 0363-0892

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

Mucus Relief Dm
NDC 0363-9013

Generic Name
Guaifenesin And Dextromethorphan Hydrobromide
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Cold, Flu And Sore Throat
NDC 0363-9016

Generic Name
Acetaminophen, Guaifenesin, Dextromethorphan Hydrobromide, A...
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Maximum Strength Cold And Flu
NDC 0363-9017

Generic Name
Acetaminophen, Guaifenesin, Dextromethorphan Hydrobromide, A...
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Maximum Strength Congestion And Headache
NDC 0363-9019

Generic Name
Acetaminophen, Dextromethorphan Hydrobromide, And Phenylephr...
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Ibuprofen
NDC 0363-9593

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

Acetaminophen Diphenhydramine Hcl
NDC 0363-9661

Generic Name
Acetaminophen Diphenhydramine Hcl
Dosage Form
Tablet
Route
Oral
Marketing
OTC MONOGRAPH DRUG
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

walgreens

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