SODIUM STEARYL FUMARATE
UNII 7CV7WJK4UI

Substance Identification & Data

This profile provides standardized clinical and technical data for Sodium Stearyl Fumarate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 7CV7WJK4UI.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 4070-80-8 and the RxNorm Concept ID (RxCUI) 1364936. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
7CV7WJK4UI
CAS Registry Number
4070-80-8
RxNorm Concept ID
1364936

Detailed Substance Profile

Preferred Name
SODIUM STEARYL FUMARATE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
7CV7WJK4UI
The specific atomic composition represented as a molecular structure string.
InChIKey
C22H39O4.Na
International Chemical Identifier digital signature for unique molecular identification.
SMILES String
STFSJTPVIIDAQX-LTRPLHCISA-M
Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
C82292
National Cancer Institute reference terminology for clinical and research data.
PubChem CID
23665634
Unique identification number in the NCBI database of chemical substances.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
C(/C=C/C(=O)OCCCCCCCCCCCCCCCCCC)([O-])=O.[Na+]

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Sodium Stearyl Fumarate. 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

SODIUM STEARYL FUMARATE

Common Names & Synonyms

FUMARIC ACID, OCTADECYL ESTER, SODIUM SALT
SODIUM STEARYL FUMARATE [EP MONOGRAPH]
SODIUM STEARYL FUMARATE [FCC]
SODIUM STEARYL FUMARATE [II]
SODIUM STEARYL FUMARATE [MART.]
SODIUM STEARYL FUMARATE [MI]
SODIUM STEARYL FUMARATE [USP-RS]
SODIUM STEARYL FUMARATE [VANDF]

Systematic Nomenclature

SODIUM MONOSTEARYL FUMARATE

NDC Products Containing SODIUM STEARYL FUMARATE

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 1
→ AbbVie Inc. 13
→ Accord Healthcare Inc. 9
→ Allergan, Inc. 2
→ Almirall, LLC 3
→ AstraZeneca Pharmaceuticals LP 5
→ Eli Lilly and Company 4
→ Endo USA, Inc. 3
→ Genentech, Inc. 3
→ Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. 1
→ Hikma Pharmaceuticals USA Inc. 6
→ L. Perrigo Company 6
→ Lannett Company, Inc. 14
→ Major Pharmaceuticals 7
→ Merck Sharp & Dohme LLC 17
→ Mylan Pharmaceuticals Inc. 9
→ NCS HealthCare of KY, Inc dba Vangard Labs 1
→ NCS HealthCare of KY, LLC dba Vangard Labs 7
→ Novartis Pharmaceuticals Corporation 1
→ PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma 4
→ Pfizer Laboratories Div Pfizer Inc 3
→ Rising Pharma Holdings, Inc. 5
→ Rite Aid 1
→ Rite Aid Corporation 3
→ Rugby Laboratories 3
→ Rugby Laboratories, Inc. 2
→ Sandoz Inc 5
→ SpecGx LLC 2
→ Sunrise Pharmaceutical, Inc. 1
→ TARGET CORPORATION 1
→ Target Corporation 4
→ Teva Pharmaceuticals USA, Inc. 24
→ Teva Pharmaceuticals, Inc. 2
→ Torrent Pharmaceuticals Limited 10
→ UP & UP 1
→ WALGREEN CO 1
→ WALGREEN CO. 4
→ Walgreen Co. 1
→ Walgreen Company 7
→ Walgreens 3
→ Walgreens Company 1

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

AbbVie Inc.

NDC Product
Human Prescription Drug

Kaletra
NDC 0074-0522

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

Venclexta
NDC 0074-0561

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

Venclexta
NDC 0074-0566

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

Venclexta
NDC 0074-0576

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

Venclexta
NDC 0074-0579

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

Mavyret
NDC 0074-2600

Generic Name
Glecaprevir And Pibrentasvir
Dosage Form
Pellet
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Mavyret
NDC 0074-2625

Generic Name
Glecaprevir And Pibrentasvir
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
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 0074-3956

Generic Name
Lopinavir And Ritonavir
Dosage Form
Solution
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
NDC Product
Human Prescription Drug

Qulipta
NDC 0074-7094

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

Qulipta
NDC 0074-7095

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

Qulipta
NDC 0074-7096

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

Accord Healthcare Inc.

NDC Product
Human Prescription Drug

Levothyroxine Sodium
NDC 16729-447

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

Levothyroxine Sodium
NDC 16729-448

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

Levothyroxine Sodium
NDC 16729-449

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

Levothyroxine Sodium
NDC 16729-450

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

Levothyroxine Sodium
NDC 16729-451

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

Levothyroxine Sodium
NDC 16729-452

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

Levothyroxine Sodium
NDC 16729-453

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

Levothyroxine Sodium
NDC 16729-454

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

Levothyroxine Sodium
NDC 16729-455

Generic Name
Levothyroxine Sodium
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

Allergan, Inc.

NDC Product
Human Prescription Drug

Ubrelvy
NDC 0023-6498

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

Ubrelvy
NDC 0023-6501

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

Almirall, LLC

NDC Product
Human Prescription Drug

Seysara
NDC 16110-245

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

Seysara
NDC 16110-246

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

Seysara
NDC 16110-247

Generic Name
Sarecycline Hydrochloride
Dosage Form
Tablet, Coated
Route
Oral
Marketing
NDA
Active Listing

AstraZeneca Pharmaceuticals LP

NDC Product
Human Prescription Drug

Lynparza
NDC 0310-0668

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

Lynparza
NDC 0310-0679

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

Tagrisso
NDC 0310-1349

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

Tagrisso
NDC 0310-1350

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

Calquence
NDC 0310-3512

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

Eli Lilly and Company

NDC Product
Human Prescription Drug

Verzenio
NDC 0002-4483

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

Verzenio
NDC 0002-4815

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

Verzenio
NDC 0002-5337

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

Verzenio
NDC 0002-6216

Generic Name
Abemaciclib
Dosage Form
Tablet
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

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

Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Diflunisal
NDC 14539-673

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

Hikma Pharmaceuticals USA Inc.

NDC Product
Human Prescription Drug

Cyclophosphamide
NDC 0054-0382

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

Cyclophosphamide
NDC 0054-0383

Generic Name
Cyclophosphamide
Dosage Form
Capsule
Route
Oral
Marketing
NDA
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

Sapropterin Dihydrochloride
NDC 0054-0906

Generic Name
Sapropterin Dihydrochloride
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

L. Perrigo Company

NDC Product
Human Otc Drug

Good Sense Lansoprazole
NDC 0113-0116

Generic Name
Lansoprazole
Dosage Form
Tablet, Orally Disintegrating, Delayed Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Otc Drug

Good Sense Omeprazole
NDC 0113-0520

Generic Name
Omeprazole
Dosage Form
Tablet, Orally Disintegrating, Delayed Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Otc Drug

Good Sense Omeprazole
NDC 0113-0915

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

Good Sense Omeprazole
NDC 0113-1723

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

Lannett Company, Inc.

NDC Product
Human Prescription Drug

Olanzapine
NDC 0527-3161

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

Olanzapine
NDC 0527-3162

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

Olanzapine
NDC 0527-3163

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

Olanzapine
NDC 0527-3164

Generic Name
Olanzapine
Dosage Form
Tablet, Orally Disintegrating
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

Major Pharmaceuticals

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 0904-6322

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

Metoprolol Succinate
NDC 0904-6323

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

Metoprolol Succinate
NDC 0904-6324

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

Linezolid
NDC 0904-6553

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

Sildenafil
NDC 0904-6671

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

Posaconazole
NDC 0904-7149

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

Ramelteon
NDC 0904-7494

Generic Name
Ramelteon
Dosage Form
Tablet
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

Januvia
NDC 0006-0112

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

Januvia
NDC 0006-0221

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

Isentress
NDC 0006-0227

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

Januvia
NDC 0006-0277

Generic Name
Sitagliptin
Dosage Form
Tablet, Film Coated
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

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
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

Delstrigo
NDC 0006-5007

Generic Name
Doravirine, Lamivudine, And Tenofovir Disoproxil Fumarate
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Steglujan
NDC 0006-5367

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

Steglujan
NDC 0006-5368

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

Mylan Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Lenalidomide
NDC 0378-1936

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

Lenalidomide
NDC 0378-1937

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

Lenalidomide
NDC 0378-1940

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

Lenalidomide
NDC 0378-1941

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

Clozapine
NDC 0378-3813

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

Clozapine
NDC 0378-3815

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

Nevirapine
NDC 0378-4890

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

Almotriptan Malate
NDC 0378-5245

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

Almotriptan Malate
NDC 0378-5246

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

NCS HealthCare of KY, Inc dba Vangard Labs

NDC Product
Human Prescription Drug

Fenofibrate
NDC 0615-8270

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

NCS HealthCare of KY, LLC dba Vangard Labs

NDC Product
Human Prescription Drug

Metoprolol Succinate
NDC 0615-7823

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

Metoprolol Succinate
NDC 0615-7824

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

Metoprolol Succinate
NDC 0615-7825

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

Celecoxib
NDC 0615-8571

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

Celecoxib
NDC 0615-8572

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

Bupropion Hydrochloride
NDC 0615-8601

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

Bupropion Hydrochloride
NDC 0615-8602

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

Novartis Pharmaceuticals Corporation

NDC Product
Human Prescription Drug

Rhapsido
NDC 0078-1483

Generic Name
Remibrutinib
Dosage Form
Tablet
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

Pfizer Laboratories Div Pfizer Inc

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

Rising Pharma Holdings, Inc.

NDC Product
Human Prescription Drug

Carbidopa And Levodopa
NDC 16571-157

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

Carbidopa And Levodopa
NDC 16571-158

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

Carbidopa And Levodopa
NDC 16571-159

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

Nateglinide
NDC 16571-758

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

Nateglinide
NDC 16571-759

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

Rite Aid

NDC Product
Human Otc Drug

Omeprazole
NDC 11822-0061

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

Rite Aid Corporation

NDC Product
Human Otc Drug

Omeprazole
NDC 11822-0915

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

Omeprazole
NDC 11822-1040

Generic Name
Omeprazole
Dosage Form
Tablet, Orally Disintegrating, Delayed Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Otc Drug

Omeprazole
NDC 11822-1190

Generic Name
Omeprazole
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
NDA
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
NDC Product
Human Otc Drug

Loratadine Odt
NDC 0536-1367

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

Rugby Omeprazole
NDC 0536-1448

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

Rugby Laboratories, Inc.

NDC Product
Human Otc Drug

Nicotine Mini
NDC 0536-1239

Generic Name
Nicotine Polacrilex
Dosage Form
Lozenge
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Mini Nicotine
NDC 0536-1241

Generic Name
Nicotine Polacrilex
Dosage Form
Lozenge
Route
Oral
Marketing
ANDA
Active Listing

Sandoz Inc

NDC Product
Human Prescription Drug

Sitagliptin Phosphate
NDC 0781-5766

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

Sitagliptin Phosphate
NDC 0781-5768

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

Sitagliptin Phosphate
NDC 0781-5770

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

Sitagliptin And Metformin Hydrochloride
NDC 0781-5801

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

Sitagliptin And Metformin Hydrochloride
NDC 0781-5802

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

SpecGx LLC

NDC Product
Human Prescription Drug

Buprenorphine Hcl
NDC 0406-7012

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

Buprenorphine Hcl
NDC 0406-7018

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

Sunrise Pharmaceutical, Inc.

NDC Product
Human Prescription Drug

Sulfasalazine
NDC 11534-201

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

TARGET CORPORATION

NDC Product
Human Otc Drug

Gas Relief - Cherry Flavor
NDC 11673-066

Generic Name
Simethicone
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Target Corporation

NDC Product
Human Otc Drug

Up And Up Omeprazole
NDC 11673-018

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

Up And Up Omeprazole
NDC 11673-212

Generic Name
Omeprazole
Dosage Form
Tablet, Orally Disintegrating, Delayed Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Otc Drug

Up And Up Omeprazole
NDC 11673-346

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

Up And Up Omeprazole
NDC 11673-915

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

Teva Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Tolterodine Tartrate
NDC 0093-0010

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

Tolterodine Tartrate
NDC 0093-0018

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

Risedronate Sodium
NDC 0093-3098

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

Risedronate Sodium
NDC 0093-3099

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

Risedronate Sodium
NDC 0093-3100

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

Olanzapine
NDC 0093-5245

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

Olanzapine
NDC 0093-5246

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

Olanzapine
NDC 0093-5247

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

Olanzapine
NDC 0093-5248

Generic Name
Olanzapine
Dosage Form
Tablet, Orally Disintegrating
Route
Oral
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
Human Prescription Drug

Clozapine
NDC 0093-5416

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

Clozapine
NDC 0093-5417

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

Clozapine
NDC 0093-5419

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

Imatinib Mesylate
NDC 0093-7629

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

Imatinib Mesylate
NDC 0093-7630

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

Famciclovir
NDC 0093-8117

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

NDC 0093-8117

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

NDC 0093-8118

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

Famciclovir
NDC 0093-8118

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

Famciclovir
NDC 0093-8119

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

NDC 0093-8119

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

Diflunisal
NDC 0093-9222

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

Clonazepam
NDC 0093-9293

Generic Name
Clonazepam
Dosage Form
Tablet, Orally Disintegrating
Route
Oral
Marketing
ANDA
Active Listing

Teva Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Dapagliflozin
NDC 0480-3527

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

Dapagliflozin
NDC 0480-3528

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

Torrent Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Felodipine
NDC 13668-132

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

Felodipine
NDC 13668-133

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

Felodipine
NDC 13668-134

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

Sildenafil
NDC 13668-185

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

Sildenafil Citrate
NDC 13668-186

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

Sildenafil Citrate
NDC 13668-187

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

Sildenafil Citrate
NDC 13668-188

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

Fenofibrate
NDC 13668-438

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

Fenofibrate
NDC 13668-439

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

Fenofibrate
NDC 13668-440

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

UP & UP

NDC Product
Human Otc Drug

Omeprazole
NDC 11673-948

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

WALGREEN CO

NDC Product
Human Otc Drug

Acetaminophen Aspirin Caffeine
NDC 0363-9680

Generic Name
Acetaminophen Aspirin Caffeine
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

WALGREEN CO.

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 0363-0361

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

Acid Reducer
NDC 0363-1008

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

Childrens Loratadine Odt
NDC 0363-4020

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

Loratadine Odt
NDC 0363-9937

Generic Name
Loratadine
Dosage Form
Tablet, Orally Disintegrating
Route
Oral
Marketing
ANDA
Active Listing

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

Omeprazole
NDC 0363-0007

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

Omeprazole And Sodium Bicarbonate
NDC 0363-0732

Generic Name
Omeprazole, Sodium Bicarbonate
Dosage Form
Capsule, Gelatin Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Omeprazole
NDC 0363-0915

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

Lansoprazole
NDC 0363-1419

Generic Name
Lansoprazole
Dosage Form
Tablet, Orally Disintegrating, Delayed Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Otc Drug

Omeprazole
NDC 0363-1819

Generic Name
Omeprazole
Dosage Form
Tablet, Orally Disintegrating, Delayed Release
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Otc Drug

Omeprazole
NDC 0363-6101

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

Omeprazole
NDC 0363-9980

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

Walgreens

NDC Product
Human Otc Drug

Nicotine Mini
NDC 0363-0262

Generic Name
Nicotine Polacrilex
Dosage Form
Lozenge
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 0363-1353

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

Mini Nicotine
NDC 0363-2640

Generic Name
Nicotine Polacrilex
Dosage Form
Lozenge
Route
Oral
Marketing
ANDA
Active Listing

Walgreens Company

NDC Product
Human Otc Drug

Omeprazole
NDC 0363-1607

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

External Clinical & Regulatory Resources

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