HYDROXYPROPYL CELLULOSE (1600000 WAMW)
UNII RFW2ET671P

Substance Identification & Data

This profile provides standardized clinical and technical data for Hydroxypropyl Cellulose (1600000 Wamw), uniquely identified by the FDA Unique Ingredient Identifier (UNII) RFW2ET671P.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 9004-64-2 and the RxNorm Concept ID (RxCUI) 1811461. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
RFW2ET671P
CAS Registry Number
9004-64-2
RxNorm Concept ID
1811461

Detailed Substance Profile

Preferred Name
HYDROXYPROPYL CELLULOSE (1600000 WAMW)
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
RFW2ET671P
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
C29139
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 Hydroxypropyl Cellulose (1600000 Wamw). 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

HYDROXYPROPYL CELLULOSE (1600000 WAMW)
HYDROXYPROPYL CELLULOSE (TYPE H)

Brand / Trade Names

KLUCEL HF
KLUCEL HXF

NDC Products Containing HYDROXYPROPYL CELLULOSE (1600000 WAMW)

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.
→ AbbVie Inc. 2
→ Actavis Pharma, Inc. 30
→ Allergan, Inc. 2
→ Amneal Pharmaceuticals of New York LLC 6
→ Astellas Pharma US, Inc. 3
→ AstraZeneca Pharmaceuticals LP 9
→ Bausch Health US LLC 5
→ Bausch Health US, LLC 4
→ Boehringer Ingelheim Pharmaceuticals, Inc. 6
→ E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC 1
→ E.R. Squibb & Sons, L.L.C. 7
→ ENDO USA, Inc. 1
→ Eli Lilly and Company 3
→ Endo USA, Inc. 3
→ Haleon US Holdings LLC 3
→ Hikma Pharmaceuticals USA Inc. 1
→ L. Perrigo Company 2
→ Merck Sharp & Dohme LLC 15
→ Mission Pharmacal Company 1
→ Mylan Pharmaceuticals Inc. 13
→ NCS HealthCare of KY, Inc dba Vangard Labs 1
→ NCS HealthCare of KY, LLC dba Vangard Labs 13
→ Padagis US LLC 5
→ Parke-Davis Div of Pfizer Inc 1
→ Person and Covey 1
→ Pfizer Laboratories Div Pfizer Inc 14
→ Sandoz Inc 1
→ Sanofi-Aventis U.S. LLC 2
→ SpecGx LLC 3
→ Teva Pharmaceuticals USA, Inc. 12
→ UCB, Inc. 6
→ WALGREEN CO. 5
→ WALGREEN COMPANY 1
→ Walgreen Co. 1
→ Walgreen Company 5
→ Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. 11
→ sanofi-aventis U.S. LLC 1

AbbVie Inc.

NDC Product
Human Prescription Drug

Norvir
NDC 0074-3399

Generic Name
Ritonavir
Dosage Form
Powder
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Kaletra
NDC 0074-6799

Generic Name
Lopinavir And Ritonavir
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing

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

Fluvoxamine Maleate
NDC 0228-2848

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

NDC 0228-2848

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

NDC 0228-2849

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

Fluvoxamine Maleate
NDC 0228-2849

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

Diltiazem Hydrochloride
NDC 0228-2918

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

Clonidine Hydrochloride
NDC 0228-4241

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

Verapamil Hydrochloride
NDC 0591-0343

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

NDC 0591-0343

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

NDC 0591-0345

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

Verapamil Hydrochloride
NDC 0591-0345

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

Verapamil Hydrochloride
NDC 0591-0404

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

NDC 0591-0404

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

NDC 0591-2191

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

Ramelteon
NDC 0591-2191

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

Bupropion Hydrochloride Xl
NDC 0591-3331

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

Bupropion Hydrochloride Sr
NDC 0591-3540

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

Bupropion Hydrochloride Sr
NDC 0591-3541

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

Bupropion Hydrochloride Sr
NDC 0591-3542

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

Bupropion Hydrochloride Sr
NDC 0591-3543

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

NDC 0591-3543

Generic Name
Bupropion Hydrochloride
Dosage Form
Tablet, Film Coated, Extended Release
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing

Allergan, Inc.

NDC Product
Human Prescription Drug

Actonel
NDC 0430-0472

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

Actonel
NDC 0430-0478

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

Amneal Pharmaceuticals of New York LLC

NDC Product
Human Prescription Drug

Carvedilol Phosphate
NDC 0115-1248

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

Carvedilol Phosphate
NDC 0115-1249

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

Carvedilol Phosphate
NDC 0115-1250

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

Carvedilol Phosphate
NDC 0115-1251

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

Bupropion Hydrochloride
NDC 0115-5445

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

Bupropion Hydrochloride
NDC 0115-6811

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

Astellas Pharma US, Inc.

NDC Product
Human Prescription Drug

Myrbetriq
NDC 0469-2601

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

Myrbetriq
NDC 0469-2602

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

Myrbetriq
NDC 0469-5020

Generic Name
Mirabegron
Dosage Form
Granule, For Suspension, Extended Release
Route
Oral
Marketing
NDA
Active Listing

AstraZeneca Pharmaceuticals LP

NDC Product
Human Prescription Drug

Brilinta
NDC 0186-0776

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

Brilinta
NDC 0186-0777

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

Nexium
NDC 0186-4010

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

Nexium
NDC 0186-4020

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

Nexium
NDC 0186-4025

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

Nexium
NDC 0186-4040

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

Nexium
NDC 0186-4050

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

Nexium
NDC 0186-5020

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

Nexium
NDC 0186-5040

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

Bausch Health US LLC

NDC Product
Human Prescription Drug

Cardizem
NDC 0187-0771

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

Cardizem
NDC 0187-0772

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

Cardizem
NDC 0187-0792

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

Pepcid
NDC 0187-4420

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

Pepcid
NDC 0187-4440

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

Bausch Health US, LLC

NDC Product
Human Prescription Drug

Efudex
NDC 0187-3204

Generic Name
Fluorouracil
Dosage Form
Cream
Route
Topical
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Retin-a
NDC 0187-5170

Generic Name
Tretinoin
Dosage Form
Gel
Route
Topical
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Retin-a
NDC 0187-5172

Generic Name
Tretinoin
Dosage Form
Gel
Route
Topical
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Targretin
NDC 0187-5525

Generic Name
Bexarotene
Dosage Form
Gel
Route
Topical
Marketing
NDA
Active Listing

Boehringer Ingelheim Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Pradaxa
NDC 0597-0425

Generic Name
Dabigatran Etexilate
Dosage Form
Pellet
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Pradaxa
NDC 0597-0430

Generic Name
Dabigatran Etexilate
Dosage Form
Pellet
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Pradaxa
NDC 0597-0435

Generic Name
Dabigatran Etexilate
Dosage Form
Pellet
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Pradaxa
NDC 0597-0440

Generic Name
Dabigatran Etexilate
Dosage Form
Pellet
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Pradaxa
NDC 0597-0445

Generic Name
Dabigatran Etexilate
Dosage Form
Pellet
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Pradaxa
NDC 0597-0450

Generic Name
Dabigatran Etexilate
Dosage Form
Pellet
Route
Oral
Marketing
NDA
Active Listing

E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Betamethasone Dipropionate
NDC 0168-0267

Generic Name
Betamethasone Dipropionate
Dosage Form
Lotion, Augmented
Route
Topical
Marketing
ANDA
Active Listing

E.R. Squibb & Sons, L.L.C.

NDC Product
Human Prescription Drug

Sprycel
NDC 0003-0524

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

Sprycel
NDC 0003-0527

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

Sprycel
NDC 0003-0528

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

Sprycel
NDC 0003-0852

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

Sprycel
NDC 0003-0855

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

Sprycel
NDC 0003-0857

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

Evotaz
NDC 0003-3641

Generic Name
Atazanavir And Cobicistat
Dosage Form
Tablet
Route
Oral
Marketing
NDA
Active Listing

ENDO USA, Inc.

NDC Product
Human Prescription Drug

Posaconazole
NDC 0254-2045

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

Eli Lilly and Company

NDC Product
Human Prescription Drug

Cialis
NDC 0002-4462

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

Cialis
NDC 0002-4463

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

Cialis
NDC 0002-4464

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

Endo USA, Inc.

NDC Product
Human Prescription Drug

Felodipine
NDC 0603-3581

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

Felodipine
NDC 0603-3582

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

Felodipine
NDC 0603-3583

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

Haleon US Holdings LLC

NDC Product
Human Otc Drug

Excedrin Migraine
NDC 0067-2039

Generic Name
Acetaminophen, Aspirin (nsaid) And Caffeine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
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

Hikma Pharmaceuticals USA Inc.

NDC Product
Human Prescription Drug

Cevimeline Hydrochloride
NDC 0054-0334

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

L. Perrigo Company

NDC Product
Human Otc Drug

Good Sense Ibuprofen Pm
NDC 0113-0050

Generic Name
Diphenhydramine Citrate, Ibuprofen
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Zephrex D
NDC 0113-0401

Generic Name
Pseudoephedrine Hydrochloride
Dosage Form
Capsule, Gelatin Coated
Route
Oral
Marketing
OTC MONOGRAPH DRUG
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

Emend
NDC 0006-0461

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

Emend
NDC 0006-0462

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

Emend
NDC 0006-0464

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

Isentress
NDC 0006-0473

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

Isentress
NDC 0006-0477

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

Emend
NDC 0006-3066

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

Isentress
NDC 0006-3080

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

Isentress
NDC 0006-3603

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

Emend
NDC 0006-3862

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

Noxafil
NDC 0085-2224

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

Noxafil
NDC 0085-4324

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

Noxafil
NDC 0085-4331

Generic Name
Posaconazole
Dosage Form
Solution
Route
Intravenous
Marketing
NDA
Active Listing

Mission Pharmacal Company

NDC Product
Human Prescription Drug

Thiola
NDC 0178-0900

Generic Name
Tiopronin
Dosage Form
Tablet, Sugar Coated
Route
Oral
Marketing
NDA
Active Listing

Mylan Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Thioridazine Hydrochloride
NDC 0378-0612

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

Thioridazine Hydrochloride
NDC 0378-0614

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

Thioridazine Hydrochloride
NDC 0378-0616

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

Thioridazine Hydrochloride
NDC 0378-0618

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

Esomeprazole Magnesium
NDC 0378-2350

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

Esomeprazole Magnesium
NDC 0378-2351

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

Lansoprazole
NDC 0378-8015

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

Lansoprazole
NDC 0378-8030

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

NCS HealthCare of KY, Inc dba Vangard Labs

NDC Product
Human Prescription Drug

Mirtazapine
NDC 0615-8268

Generic Name
Mirtazapine
Dosage Form
Tablet, Film Coated
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

Simvastatin
NDC 0615-7992

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

Simvastatin
NDC 0615-7993

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

Atorvastatin Calcium
NDC 0615-8006

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

Atorvastatin Calcium
NDC 0615-8007

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

Atorvastatin Calcium
NDC 0615-8008

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

Atorvastatin Calcium
NDC 0615-8009

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

Simvastatin
NDC 0615-8056

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

Olanzapine
NDC 0615-8243

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

Olanzapine
NDC 0615-8244

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

Olanzapine
NDC 0615-8245

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

Olanzapine
NDC 0615-8246

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

Padagis US LLC

NDC Product
Human Prescription Drug

Tretinoin
NDC 0574-2201

Generic Name
Tretinoin
Dosage Form
Cream
Route
Topical
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tretinoin
NDC 0574-2205

Generic Name
Tretinoin
Dosage Form
Cream
Route
Topical
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tretinoin
NDC 0574-2225

Generic Name
Tretinoin
Dosage Form
Cream
Route
Topical
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tretinoin
NDC 0574-2301

Generic Name
Tretinoin
Dosage Form
Gel
Route
Topical
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Tretinoin
NDC 0574-2325

Generic Name
Tretinoin
Dosage Form
Gel
Route
Topical
Marketing
ANDA
Active Listing

Parke-Davis Div of Pfizer Inc

NDC Product
Human Prescription Drug

Lopid
NDC 0071-0737

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

Person and Covey

NDC Product
Human Otc Drug

Solbar Thirty Spf 30
NDC 0096-0685

Generic Name
Solbar Thirty Spf30
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Pfizer Laboratories Div Pfizer Inc

NDC Product
Human Prescription Drug

Xeljanz Xr
NDC 0069-0501

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

Xeljanz Xr
NDC 0069-0502

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

Xeljanz
NDC 0069-1002

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

Xeljanz
NDC 0069-1029

Generic Name
Tofacitinib
Dosage Form
Solution
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Caduet
NDC 0069-2260

Generic Name
Amlodipine Besylate And Atorvastatin Calcium
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Procardia Xl
NDC 0069-2650

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

Procardia Xl
NDC 0069-2660

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

Zithromax
NDC 0069-3120

Generic Name
Azithromycin Dihydrate
Dosage Form
Powder, For Suspension
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Zithromax
NDC 0069-3130

Generic Name
Azithromycin Dihydrate
Dosage Form
Powder, For Suspension
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Zithromax
NDC 0069-3140

Generic Name
Azithromycin Dihydrate
Dosage Form
Powder, For Suspension
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Zithromax
NDC 0069-4061

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

Paxlovid
NDC 0069-5045

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

Paxlovid
NDC 0069-5317

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

Paxlovid
NDC 0069-5321

Generic Name
Nirmatrelvir And Ritonavir
Dosage Form
Kit
Route
N/A
Marketing
NDA
Active Listing

Sandoz Inc

NDC Product
Human Prescription Drug

Hydroxyzine Pamoate
NDC 0185-0674

Generic Name
Hydroxyzine Pamoate
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing

Sanofi-Aventis U.S. LLC

NDC Product
Human Prescription Drug

Plavix
NDC 0024-1171

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

Plavix
NDC 0024-1332

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

SpecGx LLC

Teva Pharmaceuticals USA, Inc.

NDC Product
Drug For Further Processing

NDC 0093-0314

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

Ketorolac Tromethamine
NDC 0093-0314

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

Azithromycin
NDC 0093-2026

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

Azithromycin
NDC 0093-2027

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

Cyclobenzaprine Hydrochloride
NDC 0093-3420

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

Cyclobenzaprine Hydrochloride
NDC 0093-3421

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

Cyclobenzaprine Hydrochloride
NDC 0093-3422

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

Pioglitazone
NDC 0093-7271

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

Pioglitazone
NDC 0093-7272

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

Pioglitazone
NDC 0093-7273

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

Clopidogrel
NDC 0093-7314

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

UCB, Inc.

NDC Product
Human Prescription Drug

Vimpat
NDC 0131-1810

Generic Name
Lacosamide
Dosage Form
Injection
Route
Intravenous
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Vimpat
NDC 0131-2477

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

Vimpat
NDC 0131-2478

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

Vimpat
NDC 0131-2479

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

Vimpat
NDC 0131-2480

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

Vimpat
NDC 0131-5410

Generic Name
Lacosamide
Dosage Form
Solution
Route
Oral
Marketing
NDA
Active Listing

WALGREEN CO.

NDC Product
Human Otc Drug

Pain Reliever
NDC 0363-0792

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

Famotidine
NDC 0363-1899

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

Famotidine
NDC 0363-4400

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

Famotidine
NDC 0363-5300

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

Famotidine
NDC 0363-9607

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

WALGREEN COMPANY

Walgreen Co.

NDC Product
Human Otc Drug

Wal-dram 2 Quick-dissolving
NDC 0363-1407

Generic Name
Meclizine Hydrochloride
Dosage Form
Tablet, Orally Disintegrating
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Walgreen Company

NDC Product
Human Otc Drug

Ibuprofen Pm
NDC 0363-0050

Generic Name
Diphenhydramine Citrate, Ibuprofen
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Salicylic Acid
NDC 0363-0219

Generic Name
Wart Remover Gel
Dosage Form
Gel
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Pain Reliever Pm Extra Strength
NDC 0363-0556

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

Loratadine And Pseudoephedrine
NDC 0363-0725

Generic Name
Loratadine And Pseudoephedrine
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Wal-zyr D
NDC 0363-0989

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

Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.

NDC Product
Human Prescription Drug

Duavee
NDC 0008-1123

Generic Name
Conjugated Estrogens/bazedoxifene
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Premarin
NDC 0046-1100

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

Premarin
NDC 0046-1101

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

Premarin
NDC 0046-1102

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

Premarin
NDC 0046-1103

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

Premarin
NDC 0046-1104

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

Prempro
NDC 0046-1105

Generic Name
Conjugated Estrogens And Medroxyprogesterone Acetate
Dosage Form
Tablet, Sugar Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Prempro
NDC 0046-1106

Generic Name
Conjugated Estrogens And Medroxyprogesterone Acetate
Dosage Form
Tablet, Sugar Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Prempro
NDC 0046-1107

Generic Name
Conjugated Estrogens And Medroxyprogesterone Acetate
Dosage Form
Tablet, Sugar Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Prempro
NDC 0046-1108

Generic Name
Conjugated Estrogens And Medroxyprogesterone Acetate
Dosage Form
Tablet, Sugar Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Premphase
NDC 0046-2575

Generic Name
Conjugated Estrogens And Medroxyprogesterone Acetate
Dosage Form
Kit
Route
N/A
Marketing
NDA
Active Listing

sanofi-aventis U.S. LLC

NDC Product
Human Prescription Drug

Priftin
NDC 0088-2102

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

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