SODIUM LAURYL SULFATE
UNII 368GB5141J

Substance Identification & Data

This profile provides standardized clinical and technical data for Sodium Lauryl Sulfate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 368GB5141J.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 151-21-3 and the RxNorm Concept ID (RxCUI) 9871. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
368GB5141J
CAS Registry Number
151-21-3
RxNorm Concept ID
9871

Detailed Substance Profile

Preferred Name
SODIUM LAURYL SULFATE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
368GB5141J
The specific atomic composition represented as a molecular structure string.
InChIKey
C12H25O4S.Na
International Chemical Identifier digital signature for unique molecular identification.
SMILES String
DBMJMQXJHONAFJ-UHFFFAOYSA-M
Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
C76733
National Cancer Institute reference terminology for clinical and research data.
PubChem CID
3423265
Unique identification number in the NCBI database of chemical substances.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
S([O-])(=O)(=O)OCCCCCCCCCCCC.[Na+]

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Sodium Lauryl Sulfate. 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 LAURYL SULFATE

Common Names & Synonyms

SODIUM LAURILSULFATE
SODIUM LAURILSULFATE [EP IMPURITY]
SODIUM LAURILSULFATE [EP MONOGRAPH]
SODIUM LAURILSULFATE [MART.]
SODIUM LAURYL SULFATE [FCC]
SODIUM LAURYL SULFATE [HSDB]
SODIUM LAURYL SULFATE [II]
SODIUM LAURYL SULFATE [JAN]
SODIUM LAURYL SULFATE [MI]
SODIUM LAURYL SULFATE [USP-RS]
SODIUM LAURYL SULFATE [VANDF]
SODIUM LAURYL SULFATE [WHO-DD]
SODIUM LAURYL SULFATE, SYNTHETIC
SULFURIC ACID MONODODECYL ESTER SODIUM SALT

Brand / Trade Names

TEXAPON K 12 P

Systematic Nomenclature

SODIUM DODECYL SULFATE
SODIUM DODECYL SULPHATE
SODIUM DODECYLSULFATE
SODIUM LAURYL SULPHATE
SODIUM MONODODECYL SULFATE
SODIUM MONODODECYL SULPHATE

Technical Codes

NSC-402488

NDC Products Containing SODIUM LAURYL SULFATE

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. 5
→ Amneal Pharmaceuticals of New York LLC 21
→ Colgate Oral Pharmaceuticals, Inc. 4
→ E.R. Squibb & Sons, L.L.C. 4
→ Eli Lilly and Company 5
→ Genentech, Inc. 3
→ Haleon US Holdings LLC 12
→ Hikma Pharmaceuticals USA Inc 2
→ Hikma Pharmaceuticals USA Inc. 23
→ L. Perrigo Company 12
→ Merck Sharp & Dohme LLC 23
→ Novartis Pharmaceuticals Corporation 14
→ Parke-Davis Div of Pfizer Inc 1
→ Person and Covey 1
→ Pfizer Laboratories Div Pfizer Inc 6
→ Sanofi-Aventis U.S. LLC 1
→ Teva Pharmaceuticals USA, Inc. 58
→ Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. 4
→ sanofi-aventis U.S. LLC 1

AbbVie Inc.

NDC Product
Human Prescription Drug

Creon
NDC 0032-1203

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

Creon
NDC 0032-1206

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

Creon
NDC 0032-1212

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

Creon
NDC 0032-1224

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

Creon
NDC 0032-3016

Generic Name
Pancrelipase
Dosage Form
Capsule, Delayed Release Pellets
Route
Oral
Marketing
BLA
Active Listing

Amneal Pharmaceuticals of New York LLC

NDC Product
Human Prescription Drug

Albendazole
NDC 0115-1701

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

Apixaban
NDC 0115-1721

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

Apixaban
NDC 0115-1722

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

Ultramicrosize Griseofulvin
NDC 0115-1724

Generic Name
Ultramicrosize Griseofulvin Tablets
Dosage Form
Tablet, Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Ultramicrosize Griseofulvin
NDC 0115-1725

Generic Name
Ultramicrosize Griseofulvin Tablets
Dosage Form
Tablet, Coated
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Methylphenidate Hydrochloride
NDC 0115-1736

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

Methylphenidate Hydrochloride
NDC 0115-1737

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

Methylphenidate Hydrochloride
NDC 0115-1738

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

Methylphenidate Hydrochloride
NDC 0115-1739

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

Methylphenidate Hydrochloride
NDC 0115-1740

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

Methylphenidate Hydrochloride
NDC 0115-1741

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

Acitretin
NDC 0115-1750

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

Acitretin
NDC 0115-1751

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

Acitretin
NDC 0115-1752

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

Acitretin
NDC 0115-1753

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

Hydroxyzine Pamoate
NDC 0115-1803

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

Hydroxyzine Pamoate
NDC 0115-1804

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

Methitest
NDC 0115-7037

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

Dextroamphetamine Sulfate Extended-release
NDC 0115-9927

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

Dextroamphetamine Sulfate Extended-release
NDC 0115-9928

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

Dextroamphetamine Sulfate Extended-release
NDC 0115-9929

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

Colgate Oral Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Prevident 5000 Plus Fruitastic
NDC 0126-0286

Generic Name
Sodium Fluoride
Dosage Form
Paste, Dentifrice
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Prevident 5000 Plus Spearmint
NDC 0126-0287

Generic Name
Sodium Fluoride
Dosage Form
Paste, Dentifrice
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Prevident Orthodefense
NDC 0126-0289

Generic Name
Sodium Fluoride
Dosage Form
Paste, Dentifrice
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Prevident 5000 Kids
NDC 0126-0311

Generic Name
Sodium Fluoride
Dosage Form
Paste, Dentifrice
Route
Dental
Marketing
UNAPPROVED DRUG OTHER
Active Listing

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

NDC Product
Human Prescription Drug

Eliquis
NDC 0003-0893

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

Eliquis
NDC 0003-0894

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

Eliquis 30-day Starter Pack
NDC 0003-3764

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

Augtyro
NDC 0003-4040

Generic Name
Repotrectinib
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing

Eli Lilly and Company

NDC Product
Human Prescription Drug

Reyvow
NDC 0002-4312

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

Reyvow
NDC 0002-4491

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

Genentech, Inc.

NDC Product
Human Prescription Drug

Cellcept
NDC 0004-0259

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

Cellcept
NDC 0004-0261

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

Cellcept
NDC 0004-0298

Generic Name
Mycophenolate Mofetil Hydrochloride
Dosage Form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing
NDA
Active Listing

Haleon US Holdings LLC

NDC Product
Human Otc Drug

Excedrin Extra Strength Headache
NDC 0067-2003

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

Perdiem
NDC 0067-8143

Generic Name
Sennosides, Stimulant Laxative
Dosage Form
Tablet
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Excedrin Extra Strength Pain Reliever
NDC 0067-8202

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

Excedrin Extra Strength Pain Reliever
NDC 0067-8203

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

Citrucel
NDC 0135-0199

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

Alli
NDC 0135-0461

Generic Name
Orlistat
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Otc Drug

Sensodyne Repair And Protect
NDC 0135-0548

Generic Name
Stannous Fluoride
Dosage Form
Paste
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Hikma Pharmaceuticals USA Inc

NDC Product
Human Prescription Drug

Febuxostat
NDC 0054-0413

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

Febuxostat
NDC 0054-0414

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

Hikma Pharmaceuticals USA Inc.

NDC Product
Human Prescription Drug

Lithium Carbonate
NDC 0054-0021

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

Zaleplon
NDC 0054-0084

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

Zaleplon
NDC 0054-0085

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

Cevimeline Hydrochloride
NDC 0054-0334

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

Rufinamide
NDC 0054-0425

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

Rufinamide
NDC 0054-0426

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

Alvimopan
NDC 0054-0668

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

Dicyclomine Hydrochloride
NDC 0054-0748

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

Lithium Carbonate
NDC 0054-2526

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

Lithium Carbonate
NDC 0054-2527

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

Lithium Carbonate
NDC 0054-2531

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

Furosemide
NDC 0054-3294

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

Furosemide
NDC 0054-3298

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

Furosemide
NDC 0054-4297

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

Furosemide
NDC 0054-4299

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

Furosemide
NDC 0054-4301

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

Lithium Carbonate
NDC 0054-4527

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

Furosemide
NDC 0054-8297

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

Furosemide
NDC 0054-8299

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

Furosemide
NDC 0054-8301

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

Lithium Carbonate
NDC 0054-8526

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

Lithium Carbonate
NDC 0054-8527

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

Lithium Carbonate
NDC 0054-8528

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

L. Perrigo Company

NDC Product
Human Otc Drug

Good Sense Esomeprazole Magnesium
NDC 0113-0651

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

Good Sense Esomeprazole Magnesium
NDC 0113-0898

Generic Name
Esomeprazole
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
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 Lansoprazole
NDC 0113-1114

Generic Name
Lansoprazole
Dosage Form
Capsule, Delayed Release
Route
Oral
Marketing
ANDA
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
NDC Product
Human Otc Drug

Good Sense Esomeprazole Magnesium
NDC 0113-2022

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

Good Sense Childrens Ibuprofen
NDC 0113-2461

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

Good Sense Childrens Ibuprofen
NDC 0113-6040

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

Prevacid 24 Hr
NDC 0113-6117

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

Good Sense Childrens Ibuprofen
NDC 0113-7366

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

Merck Sharp & Dohme LLC

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

Zolinza
NDC 0006-0568

Generic Name
Vorinostat
Dosage Form
Capsule
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

Zepatier
NDC 0006-3074

Generic Name
Elbasvir And Grazoprevir
Dosage Form
Tablet, Film Coated
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

Verquvo
NDC 0006-5028

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

Verquvo
NDC 0006-5029

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

Verquvo
NDC 0006-5030

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

Segluromet
NDC 0006-5369

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

Segluromet
NDC 0006-5370

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

Segluromet
NDC 0006-5373

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

Segluromet
NDC 0006-5374

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

Temodar
NDC 0085-1366

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

Temodar
NDC 0085-1381

Generic Name
Temozolomide
Dosage Form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Temodar
NDC 0085-1417

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

Temodar
NDC 0085-1425

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

Temodar
NDC 0085-1430

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

Temodar
NDC 0085-1519

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

Temodar
NDC 0085-3004

Generic Name
Temozolomide
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing

Novartis Pharmaceuticals Corporation

NDC Product
Human Prescription Drug

Exjade
NDC 0078-0468

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

Exjade
NDC 0078-0469

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

Exjade
NDC 0078-0470

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

Tegretol Xr
NDC 0078-0510

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

Tegretol Xr
NDC 0078-0511

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

Tegretol Xr
NDC 0078-0512

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

Jadenu
NDC 0078-0655

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

Jadenu
NDC 0078-0656

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

Tabrecta
NDC 0078-0709

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

Jadenu
NDC 0078-0713

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

Tabrecta
NDC 0078-0716

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

Jadenu
NDC 0078-0720

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

Jadenu
NDC 0078-0727

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

Rhapsido
NDC 0078-1483

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

Parke-Davis Div of Pfizer Inc

NDC Product
Human Prescription Drug

Celontin
NDC 0071-0525

Generic Name
Methsuximide
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing

Person and Covey

NDC Product
Human Otc Drug

Aquanil Hc
NDC 0096-0732

Generic Name
Hydrocortisone
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Pfizer Laboratories Div Pfizer Inc

NDC Product
Human Prescription Drug

Zithromax
NDC 0069-3060

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

Zithromax
NDC 0069-3070

Generic Name
Azithromycin Dihydrate
Dosage Form
Tablet, Film Coated
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

Sanofi-Aventis U.S. LLC

NDC Product
Human Prescription Drug

Fexinidazole
NDC 0024-4512

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

Teva Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Piroxicam
NDC 0093-0756

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

Piroxicam
NDC 0093-0757

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

Nortriptyline Hydrochloride
NDC 0093-0810

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

Nortriptyline Hydrochloride
NDC 0093-0811

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

Nortriptyline Hydrochloride
NDC 0093-0812

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

Nortriptyline Hydrochloride
NDC 0093-0813

Generic Name
Nortriptyline Hydrochloride
Dosage Form
Capsule
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

Acitretin
NDC 0093-1135

Generic Name
Acitretin
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0093-1135

Generic Name
Acitretin
Dosage Form
Capsule
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Drug For Further Processing

NDC 0093-1136

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

Acitretin
NDC 0093-1136

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

Acitretin
NDC 0093-1138

Generic Name
Acitretin
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0093-1138

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

Doxazosin
NDC 0093-2067

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

Doxazosin
NDC 0093-2068

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

Doxazosin
NDC 0093-2069

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

Doxazosin
NDC 0093-2070

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

Amoxicillin
NDC 0093-2267

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

Amoxicillin
NDC 0093-2268

Generic Name
Amoxicillin
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0093-3002

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

Quinine Sulfate
NDC 0093-3002

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

Amoxicillin
NDC 0093-3109

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

Dicloxacillin Sodium
NDC 0093-3123

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

Dicloxacillin Sodium
NDC 0093-3125

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

Disopyramide Phosphate
NDC 0093-3127

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

Disopyramide Phosphate
NDC 0093-3129

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

Cephalexin
NDC 0093-3145

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

Cephalexin
NDC 0093-3147

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

Cefdinir
NDC 0093-3160

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

Cefadroxil
NDC 0093-3196

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

Estradiol
NDC 0093-3541

Generic Name
Estradiol
Dosage Form
Cream
Route
Vaginal
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Atomoxetine
NDC 0093-3542

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

Atomoxetine
NDC 0093-3543

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

Atomoxetine
NDC 0093-3544

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

Atomoxetine
NDC 0093-3545

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

Atomoxetine
NDC 0093-3546

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

Atomoxetine
NDC 0093-3547

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

Atomoxetine
NDC 0093-3548

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

Acyclovir
NDC 0093-3630

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

Amoxicillin
NDC 0093-4155

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

Cephalexin
NDC 0093-4175

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

Cephalexin
NDC 0093-4177

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

Atazanavir Sulfate
NDC 0093-5526

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

Atazanavir Sulfate
NDC 0093-5527

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

Atazanavir Sulfate
NDC 0093-5528

Generic Name
Atazanavir Sulfate
Dosage Form
Capsule
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

Clopidogrel
NDC 0093-7314

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

Erlotinib
NDC 0093-7663

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

Erlotinib
NDC 0093-7664

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

Tiopronin
NDC 0093-7909

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

NDC 0093-7909

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

Cimetidine
NDC 0093-8192

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

NDC 0093-8192

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

Cimetidine
NDC 0093-8204

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

NDC 0093-8204

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

Cimetidine
NDC 0093-8305

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

NDC 0093-8305

Generic Name
Cimetidine
Dosage Form
Tablet, Film Coated
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing

Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.

NDC Product
Human Prescription Drug

Protonix Delayed-release
NDC 0008-0841

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

Protonix Delayed-release
NDC 0008-0843

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

Protonix Delayed-release
NDC 0008-0844

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

Premarin Vaginal
NDC 0046-0872

Generic Name
Conjugated Estrogens
Dosage Form
Cream
Route
Vaginal
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

External Clinical & Regulatory Resources

CAS
Common Chemistry
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NLM
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