POLYETHYLENE GLYCOL 4000
UNII 4R4HFI6D95

Substance Identification & Data

This profile provides standardized clinical and technical data for Polyethylene Glycol 4000, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 4R4HFI6D95.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 25322-68-3 and the RxNorm Concept ID (RxCUI) 1310594. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
4R4HFI6D95
CAS Registry Number
25322-68-3
RxNorm Concept ID
1310594

Detailed Substance Profile

Preferred Name
POLYETHYLENE GLYCOL 4000
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
4R4HFI6D95
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
C84081
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 Polyethylene Glycol 4000. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.

FDA Official Name

PEG-90

Common Names & Synonyms

CARBOWAX 4000
MACROGOL 4000
MACROGOL 4000 [JAN]
MACROGOL 4000 [WHO-DD]
PEG 4000
PEG-85
POLYETHYLENE GLYCOL 4000
POLYETHYLENE GLYCOL 4000 [II]
POLYETHYLENE GLYCOL 4000 [USP-RS]
POLYETHYLENE GLYCOL 4000 [VANDF]

Brand / Trade Names

FORLAX
LIPOXOL 4000 MED
PLURACARE E 4000
POLYGLYKOL 4000
SABOPEG 4000
SYMPATENS-PEG/4000 G
TOHO PEG NO. 4000
UNIPEG-4000 X

NDC Products Containing POLYETHYLENE GLYCOL 4000

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.
→ 7-ELEVEN, INC. 1
→ 7-Eleven 1
→ A-S Medication Solutions 18
→ Accord Healthcare Inc. 9
→ Accord Healthcare, Inc., 1
→ Actavis Pharma, Inc. 1
→ Alembic Pharmaceuticals Limited 12
→ AvKARE 4
→ BI-MART 1
→ BRACCO DIAGNOSTICS INC 2
→ Better Living Brands, LLC 1
→ Bi-Mart 1
→ Camber Pharmaceuticals, Inc. 7
→ Cranbury Pharmaceuticals, LLC 8
→ Dr. Reddy's Laboratories Inc., 4
→ Dr.Reddys Laboratories Inc 3
→ EPIC PHARMA LLC 3
→ Eli Lilly and Company 6
→ Epic Pharma, LLC 3
→ Hisun Pharmaceuticals USA, Inc. 1
→ KROGER COMPANY 2
→ Lannett Company, Inc. 1
→ Laurus Labs Limited 3
→ Major Pharmaceuticals 19
→ Micro Labs Limited 1
→ Mylan Pharmaceuticals Inc. 1
→ NCS HealthCare of KY, LLC dba Vangard Labs 1
→ Nantong Health & Beyond Hygienic Products Inc. 1
→ NorthStar Rx LLC 3
→ Novartis Pharmaceuticals Corporation 12
→ PD-Rx Pharmaceuticals, Inc. 2
→ Par Health USA, LLC 6
→ QPharma Inc 1
→ Rising Pharma Holdings, Inc. 3
→ Rugby Laboratories 1
→ SAFEWAY 1
→ Sun Pharmaceutical Industries, Inc. 6
→ TOPCO ASSOCIATES LLC 1
→ Teva Pharmaceuticals USA, Inc. 18
→ Teva Pharmaceuticals, Inc. 13
→ Torrent Pharmaceuticals Limited 3
→ Unichem Pharmaceuticals (USA), Inc. 2
→ Upsher-Smith Laboratories, LLC 9
→ WAL-MART STORES INC 1
→ WALGREEN CO. 1
→ Wal-Mart Stores, Inc. 1

7-ELEVEN, INC.

7-Eleven

NDC Product
Human Otc Drug

Acid Reducer
NDC 10202-722

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

A-S Medication Solutions

NDC Product
Human Prescription Drug

Amoxicillin And Clavulanate Potassium
NDC 50090-0820

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

Amoxicillin And Clavulanate Potassium
NDC 50090-0822

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

Famotidine
NDC 50090-1044

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

Amoxicillin And Clavulanate Potassium
NDC 50090-1809

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

Quetiapine Fumarate
NDC 50090-3333

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

Amoxicillin And Clavulanate Potassium
NDC 50090-4413

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

Memantine Hydrochloride
NDC 50090-4434

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

Potassium Chloride
NDC 50090-5335

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

Quetiapine Fumarate
NDC 50090-5473

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

Quetiapine Fumarate
NDC 50090-5884

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

Memantine Hydrochloride
NDC 50090-5926

Generic Name
Memantine Hydrochloride
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
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

Hydroxychloroquine Sulfate
NDC 50090-6280

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

Metoprolol Succinate
NDC 50090-6448

Generic Name
Metoprolol Succinate
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

Accord Healthcare Inc.

NDC Product
Human Prescription Drug

Quetiapine Fumarate
NDC 16729-132

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

Vilazodone Hydrochloride
NDC 16729-352

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

Vilazodone Hydrochloride
NDC 16729-353

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

Vilazodone Hydrochloride
NDC 16729-354

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

Pirfenidone
NDC 16729-467

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

Pirfenidone
NDC 16729-468

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

Accord Healthcare, Inc.,

NDC Product
Human Prescription Drug

Hydroxychloroquine Sulfate
NDC 16729-485

Generic Name
Hydroxychloroquine Sulfate
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Actavis Pharma, Inc.

NDC Product
Human Prescription Drug

Trospium Chloride
NDC 0591-3636

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

Alembic Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Olmesartan Medoxomil
NDC 46708-131

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

Olmesartan Medoxomil
NDC 46708-132

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

Olmesartan Medoxomil
NDC 46708-133

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

Irbesartan And Hydrochlorothiazide
NDC 46708-444

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

Zolmitriptan
NDC 46708-462

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

Zolmitriptan
NDC 46708-463

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

Sacubitril And Valsartan
NDC 46708-556

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

Sacubitril And Valsartan
NDC 46708-557

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

Sacubitril And Valsartan
NDC 46708-558

Generic Name
Sacubitril And Valsartan
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

AvKARE

NDC Product
Human Prescription Drug

Azithromycin
NDC 42291-044

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

Letrozole
NDC 42291-374

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

Potassium Chloride
NDC 42291-487

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

Valganciclovir
NDC 42291-973

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

BI-MART

NDC Product
Human Otc Drug

Ibuprofen
NDC 37835-585

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

BRACCO DIAGNOSTICS INC

NDC Product
Human Prescription Drug

Lumason
NDC 0270-7099

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

Lumason
NDC 0270-7099

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

Better Living Brands, LLC

Bi-Mart

NDC Product
Human Otc Drug

Acid Reducer
NDC 37835-189

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

Camber Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Prucalopride
NDC 31722-391

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

Prucalopride
NDC 31722-392

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

Lacosamide
NDC 31722-627

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

Lacosamide
NDC 31722-812

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

Lacosamide
NDC 31722-813

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

Lacosamide
NDC 31722-814

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

Lacosamide
NDC 31722-815

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

Cranbury Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Levetiracetam
NDC 27808-263

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

Levetiracetam
NDC 27808-264

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

Levetiracetam
NDC 27808-265

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

Levetiracetam
NDC 27808-266

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

Metoprolol Succinate
NDC 27808-302

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

Metoprolol Succinate
NDC 27808-303

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

Metoprolol Succinate
NDC 27808-304

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

Metoprolol Succinate
NDC 27808-305

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

Dr. Reddy's Laboratories Inc.,

NDC Product
Human Prescription Drug

Eltrombopag
NDC 43598-151

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

Eltrombopag
NDC 43598-730

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

Eltrombopag
NDC 43598-731

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

Eltrombopag
NDC 43598-732

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

Dr.Reddys Laboratories Inc

NDC Product
Human Prescription Drug

Saxagliptin And Metformin Hydrochloride
NDC 43598-618

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

Saxagliptin And Metformin Hydrochloride
NDC 43598-619

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

Saxagliptin And Metformin Hydrochloride
NDC 43598-620

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

EPIC PHARMA LLC

NDC Product
Human Prescription Drug

Tapentadol Hydrochloride
NDC 42806-626

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

Tapentadol Hydrochloride
NDC 42806-627

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

Tapentadol Hydrochloride
NDC 42806-628

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

Eli Lilly and Company

NDC Product
Human Prescription Drug

Foundayo
NDC 0002-4178

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

Foundayo
NDC 0002-4503

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

Foundayo
NDC 0002-4794

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

Foundayo
NDC 0002-4803

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

Foundayo
NDC 0002-4839

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

Foundayo
NDC 0002-4953

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

Epic Pharma, LLC

NDC Product
Human Prescription Drug

Labetalol Hydrochloride
NDC 42806-327

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

Labetalol Hydrochloride
NDC 42806-328

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

Labetalol Hydrochloride
NDC 42806-329

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

Hisun Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Ticagrelor
NDC 42658-115

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

KROGER COMPANY

NDC Product
Human Otc Drug

Acid Reducer
NDC 30142-077

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

Lannett Company, Inc.

NDC Product
Human Prescription Drug

Entacapone
NDC 0527-1830

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

Laurus Labs Limited

NDC Product
Human Prescription Drug

Sacubitril And Valsartan
NDC 42385-930

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

Sacubitril And Valsartan
NDC 42385-931

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

Sacubitril And Valsartan
NDC 42385-932

Generic Name
Sacubitril And Valsartan
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Major Pharmaceuticals

NDC Product
Human Prescription Drug

Quetiapine
NDC 0904-6638

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

Quetiapine
NDC 0904-6639

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

Quetiapine
NDC 0904-6640

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

Quetiapine
NDC 0904-6641

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

Quetiapine
NDC 0904-6642

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

Quetiapine
NDC 0904-6643

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

Levetiracetam
NDC 0904-7123

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

Levetiracetam
NDC 0904-7124

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

Levetiracetam
NDC 0904-7125

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

Potassium Chloride
NDC 0904-7216

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

Moxifloxacin Hydrochloride
NDC 0904-7407

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

Lacosamide
NDC 0904-7463

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

Lacosamide
NDC 0904-7464

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

Ranolazine
NDC 0904-7506

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

Sacubitril And Valsartan
NDC 0904-7580

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

Sacubitril And Valsartan
NDC 0904-7581

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

Sacubitril And Valsartan
NDC 0904-7582

Generic Name
Sacubitril And Valsartan
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Micro Labs Limited

NDC Product
Human Prescription Drug

Sevelamer Carbonate
NDC 42571-378

Generic Name
Sevelamer Carbonate
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Mylan Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Sorafenib Tosylate
NDC 0378-1201

Generic Name
Sorafenib
Dosage Form
Tablet, Film Coated
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

Nantong Health & Beyond Hygienic Products Inc.

NDC Product
Human Otc Drug

Oral Pain Relief
NDC 43473-100

Generic Name
Benzocaine
Dosage Form
Gel
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

NorthStar Rx LLC

NDC Product
Human Prescription Drug

Amoxicillin And Clavulanate Potassium
NDC 16714-295

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

Amoxicillin And Clavulanate Potassium
NDC 16714-296

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

Amoxicillin And Clavulanate Potassium
NDC 16714-297

Generic Name
Amoxicillin And Clavulanate Potassium
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Novartis Pharmaceuticals Corporation

NDC Product
Human Prescription Drug

Gleevec
NDC 0078-0401

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

Gleevec
NDC 0078-0649

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

Entresto
NDC 0078-0659

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

Entresto
NDC 0078-0696

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

Piqray
NDC 0078-0701

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

Piqray
NDC 0078-0708

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

Piqray
NDC 0078-0715

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

Entresto
NDC 0078-0777

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

Vijoice
NDC 0078-1021

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

Vijoice
NDC 0078-1028

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

Vijoice
NDC 0078-1035

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

Rhapsido
NDC 0078-1483

Generic Name
Remibrutinib
Dosage Form
Tablet
Route
Oral
Marketing
NDA
Active Listing

PD-Rx Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Levetiracetam
NDC 43063-617

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

Diclofenac Potassium
NDC 43063-848

Generic Name
Diclofenac Potassium
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
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

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

QPharma Inc

NDC Product
Human Prescription Drug

Losartan Potassium And Hydrochlorothiazide
NDC 42708-036

Generic Name
Losartan Potassium And Hydrochlorothiazide
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

Rising Pharma Holdings, Inc.

NDC Product
Human Prescription Drug

Zolmitriptan
NDC 16571-803

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

Zolmitriptan
NDC 16571-804

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

Probenecid
NDC 16571-831

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

Rugby Laboratories

NDC Product
Human Otc Drug

Acid Reducer
NDC 0536-1322

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

SAFEWAY

NDC Product
Human Otc Drug

Famotidine
NDC 21130-191

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

Sun Pharmaceutical Industries, Inc.

NDC Product
Human Prescription Drug

Quetiapine Fumarate
NDC 47335-902

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

Quetiapine Fumarate
NDC 47335-903

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

Quetiapine Fumarate
NDC 47335-904

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

Quetiapine Fumarate
NDC 47335-905

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

Quetiapine Fumarate
NDC 47335-906

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

Quetiapine Fumarate
NDC 47335-907

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

TOPCO ASSOCIATES LLC

NDC Product
Human Otc Drug

Ibuprofen
NDC 36800-663

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

Teva Pharmaceuticals USA, Inc.

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

Etodolac
NDC 0093-1118

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

Etodolac
NDC 0093-1122

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

Tramadol Hydrochloride
NDC 0093-3301

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

Etodolac
NDC 0093-7172

Generic Name
Etodolac
Dosage Form
Tablet, Film Coated, Extended Release
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

Clopidogrel
NDC 0093-7314

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

Losartan Potassium And Hydrochlorothiazide
NDC 0093-7367

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

Losartan Potassium And Hydrochlorothiazide
NDC 0093-7368

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

Losartan Potassium And Hydrochlorothiazide
NDC 0093-7369

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

Fluvastatin Sodium
NDC 0093-7446

Generic Name
Fluvastatin Sodium
Dosage Form
Tablet, Film Coated, 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

Letrozole
NDC 0093-7620

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

Famotidine
NDC 0172-5728

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

Famotidine
NDC 0172-5729

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

Aviane
NDC 0555-9045

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

Teva Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Ticagrelor
NDC 0480-2688

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

Ticagrelor
NDC 0480-2695

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

Ferric Citrate
NDC 0480-2996

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

Alvaiz
NDC 0480-3273

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

Alvaiz
NDC 0480-3274

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

Alvaiz
NDC 0480-3275

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

Alvaiz
NDC 0480-3276

Generic Name
Eltrombopag
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
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

Torrent Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Sacubitril And Valsartan
NDC 13668-634

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

Sacubitril And Valsartan
NDC 13668-635

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

Sacubitril And Valsartan
NDC 13668-636

Generic Name
Sacubitril And Valsartan
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Unichem Pharmaceuticals (USA), Inc.

NDC Product
Human Prescription Drug

Memantine Hydrochloride
NDC 29300-171

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

Memantine Hydrochloride
NDC 29300-172

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

Upsher-Smith Laboratories, LLC

NDC Product
Human Prescription Drug

Klor-con
NDC 0245-0836

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

Morphine Sulfate
NDC 0832-0225

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

Morphine Sulfate
NDC 0832-0226

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

Morphine Sulfate
NDC 0832-0227

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

Morphine Sulfate
NDC 0832-0228

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

Morphine Sulfate
NDC 0832-0229

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

Morphine Sulfate
NDC 0832-0230

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

Morphine Sulfate
NDC 0832-0233

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

Potassium Chloride
NDC 24979-230

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

WAL-MART STORES INC

WALGREEN CO.

NDC Product
Human Otc Drug

Acid Reducer
NDC 0363-1008

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

Wal-Mart Stores, Inc.

NDC Product
Human Otc Drug

Acid Reducer
NDC 49035-983

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

External Clinical & Regulatory Resources

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