AMMONIA
UNII 5138Q19F1X

Substance Identification & Data

This profile provides standardized clinical and technical data for Ammonia, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 5138Q19F1X.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 7664-41-7 and the RxNorm Concept ID (RxCUI) 1299884. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
5138Q19F1X
CAS Registry Number
7664-41-7
RxNorm Concept ID
1299884

Detailed Substance Profile

Preferred Name
AMMONIA
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
5138Q19F1X
The specific atomic composition represented as a molecular structure string.
InChIKey
H3N
International Chemical Identifier digital signature for unique molecular identification.
SMILES String
QGZKDVFQNNGYKY-UHFFFAOYSA-N
Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
C76698
National Cancer Institute reference terminology for clinical and research data.
PubChem CID
222
Unique identification number in the NCBI database of chemical substances.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
N

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Ammonia. 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

AMMONIA
AMMONIUM HYDROXIDE

Common Names & Synonyms

AMMONIA [HSDB]
AMMONIA [II]
AMMONIA [MART.]
AMMONIA [MI]
AMMONIA [VANDF]
AMMONIA [WHO-DD]
AMMONIA GAS
AMMONIA SOLUTION
AMMONIA SOLUTION [FCC]
AMMONIA SOLUTION [II]
AMMONIA SOLUTION, CONCENTRATED [EP Monograph]
AMMONIA SOLUTION, STRONG
AMMONIA SOLUTION, STRONG [II]
AMMONIA WATER
AMMONIA WATER [JAN]
AMMONIA WATER [MI]
AMMONIA WATER [WHO-DD]
AMMONIA,AROMATIC
AMMONIA,AROMATIC [VANDF]
AMMONIA-14N
AMMONIA-SOLUTION
AMMONIUM CAUSTICUM
AMMONIUM CAUSTICUM [HPUS]
AMMONIUM HYDROXIDE [HSDB]
AMMONIUM HYDROXIDE [II]
AMMONIUM HYDROXIDE [VANDF]
AMMONIUM WATER
AQUA AMMONIA
AQUEOUS AMMONIA
BUSAN 1474
HYDROGEN NITRIDE (H3N)
HYDROGEN NITRIDE (H3N2)
NITRO-SIL
SPIRIT OF HARTSHORN
STRONG AMMONIA SOLUTION
STRONG-AMMONIA SOLUTION

Brand / Trade Names

R 717 (AMMONIA)
REFRIGERENT R717

Technical Codes

E-527
INS NO.527
INS-527
MESH ID: D000641
R 717

NDC Products Containing AMMONIA

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. 1
→ Actavis Pharma, Inc. 12
→ Amneal Pharmaceuticals of New York LLC 16
→ AstraZeneca Pharmaceuticals LP 2
→ Bayer HealthCare LLC 1
→ Bayer Healthcare LLC 1
→ C.B. Fleet Company, Inc. 1
→ Crown Laboratories 1
→ E.R. Squibb & Sons, L.L.C. 3
→ Eli Lilly and Company 2
→ Endo USA, Inc. 5
→ Galderma Laboratories, L.P. 1
→ Genentech, Inc. 4
→ Haleon US Holdings LLC 12
→ Hikma Pharmaceuticals USA Inc. 15
→ Humco Holding Group, Inc. 1
→ L. Perrigo Company 3
→ Merck Sharp & Dohme LLC 11
→ Mylan Pharmaceuticals Inc. 46
→ Novartis Pharmaceuticals Corporation 1
→ Par Health USA, LLC 1
→ Pfizer Laboratories Div Pfizer Inc 10
→ SpecGx LLC 3
→ Teva Pharmaceuticals USA, Inc. 15
→ Teva Pharmaceuticals, Inc. 16
→ WALGREEN CO. 3
→ WALGREENS 2
→ WALGREENS CO. 1
→ Walgreen Company 5
→ Walgreens 3
→ Walgreens Company 2

AbbVie Inc.

NDC Product
Human Prescription Drug

Oriahnn
NDC 0074-1017

Generic Name
Elagolix And Estradiol And Norethisterone
Dosage Form
Kit
Route
N/A
Marketing
NDA
Active Listing

Actavis Pharma, Inc.

NDC Product
Human Prescription Drug

Duloxetine
NDC 0228-2890

Generic Name
Duloxetine
Dosage Form
Capsule, Delayed Release Pellets
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0228-2890

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

NDC 0228-2891

Generic Name
Duloxetine
Dosage Form
Capsule, Delayed Release Pellets
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Duloxetine
NDC 0228-2891

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

Duloxetine
NDC 0228-2892

Generic Name
Duloxetine
Dosage Form
Capsule, Delayed Release Pellets
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Drug For Further Processing

NDC 0228-2892

Generic Name
Duloxetine
Dosage Form
Capsule, Delayed Release Pellets
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing
NDC Product
Human Prescription Drug

Morphine Sulfate
NDC 0228-3090

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

Morphine Sulfate
NDC 0228-3091

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

Morphine Sulfate
NDC 0228-3092

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

Morphine Sulfate
NDC 0228-3093

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

Morphine Sulfate
NDC 0228-3116

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

Morphine Sulfate
NDC 0228-3117

Generic Name
Morphine Sulfate
Dosage Form
Capsule, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Amneal Pharmaceuticals of New York LLC

NDC Product
Human Prescription Drug

Morphine Sulfate
NDC 0115-1277

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

Morphine Sulfate
NDC 0115-1278

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

Morphine Sulfate
NDC 0115-1279

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

Morphine Sulfate
NDC 0115-1280

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

Morphine Sulfate
NDC 0115-1281

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

Morphine Sulfate
NDC 0115-1282

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

Fenofibric Acid
NDC 0115-1324

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

Fenofibric Acid
NDC 0115-1325

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

Morphine Sulfate
NDC 0115-1479

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

Tamsulosin Hydrochloride
NDC 0115-8211

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

AstraZeneca Pharmaceuticals LP

NDC Product
Human Prescription Drug

Koselugo
NDC 0310-0610

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

Koselugo
NDC 0310-0625

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

Bayer HealthCare LLC

NDC Product
Human Otc Drug

Aleve Arthritis Pain Gel
NDC 0280-0039

Generic Name
Diclofenac Sodium
Dosage Form
Gel
Route
Topical
Marketing
ANDA
Active Listing

Bayer Healthcare LLC

NDC Product
Human Otc Drug

Aleve Liquid Gels
NDC 0280-0105

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

C.B. Fleet Company, Inc.

NDC Product
Human Otc Drug

Fleet
NDC 0132-0401

Generic Name
Bisacodyl
Dosage Form
Tablet, Coated
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Crown Laboratories

NDC Product
Human Otc Drug

Mineral Ice Pain Relieving
NDC 0316-0226

Generic Name
Menthol
Dosage Form
Gel
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

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

NDC Product
Human Prescription Drug

Reyataz
NDC 0003-3622

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

Reyataz
NDC 0003-3631

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

Reyataz
NDC 0003-3638

Generic Name
Atazanavir
Dosage Form
Powder
Route
Oral
Marketing
NDA
Active Listing

Eli Lilly and Company

NDC Product
Human Prescription Drug

Retevmo
NDC 0002-2980

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

Retevmo
NDC 0002-3977

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

Endo USA, Inc.

NDC Product
Human Prescription Drug

Nitisinone
NDC 0254-3020

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

Nitisinone
NDC 0254-3021

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

Nitisinone
NDC 0254-3022

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

Tiopronin
NDC 0254-3034

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

Tiopronin
NDC 0254-3035

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

Galderma Laboratories, L.P.

NDC Product
Human Otc Drug

Differin Acne Clearing Body
NDC 0299-4132

Generic Name
Salicylic Acid
Dosage Form
Aerosol, Spray
Route
Topical
Marketing
OTC MONOGRAPH DRUG
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 0004-0260

Generic Name
Mycophenolate Mofetil
Dosage Form
Tablet, Film Coated
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

Gas-x Total Relief Maximum Strength
NDC 0067-0118

Generic Name
Calcium Carbonate, Simethicone
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Gas-x Total Relief Maximum Strength
NDC 0067-0119

Generic Name
Calcium Carbonate, Simethicone
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Voltaren Arthritis Pain
NDC 0067-8152

Generic Name
Diclofenac Sodium
Dosage Form
Gel
Route
Topical
Marketing
NDA
Active Listing
NDC Product
Human Otc Drug

Voltaren Arthritis Pain
NDC 0067-8153

Generic Name
Diclofenac Sodium
Dosage Form
Kit
Route
N/A
Marketing
NDA
Active Listing
NDC Product
Human Otc Drug

Tums Chewy Bites
NDC 0135-0183

Generic Name
Calcium Carbonate
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Tums Chewy Bites Berry Shake
NDC 0135-0184

Generic Name
Calcium Carbonate
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Tums Chewy Bites
NDC 0135-0606

Generic Name
Calcium Carbonate
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Tums Chewy Bites
NDC 0135-0618

Generic Name
Calcium Carbonate
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Tums Chewy Bites Peppermint
NDC 0135-0623

Generic Name
Calcium Carbonate
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Tums Chewy Bites With Gas Relief
NDC 0135-0624

Generic Name
Calcium Carbonate And Simethicone
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Tums Chewy Bites Mixed Fruit
NDC 0135-0641

Generic Name
Calcium Carbonate
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Tums Chewy Bites Orange And Cream Es
NDC 0135-0642

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

Hikma Pharmaceuticals USA Inc.

NDC Product
Human Prescription Drug

Balsalazide Disodium
NDC 0054-0079

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

Mycophenolate Mofetil
NDC 0054-0163

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

Mycophenolate Mofetil
NDC 0054-0166

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

Lisdexamfetamine Dimesylate
NDC 0054-0370

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

Lisdexamfetamine Dimesylate
NDC 0054-0371

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

Lisdexamfetamine Dimesylate
NDC 0054-0372

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

Lisdexamfetamine Dimesylate
NDC 0054-0373

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

Lisdexamfetamine Dimesylate
NDC 0054-0374

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

Lisdexamfetamine Dimesylate
NDC 0054-0375

Generic Name
Lisdexamfetamine Dimesylate
Dosage Form
Capsule
Route
Oral
Marketing
ANDA
Active Listing
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

Icosapent Ethyl
NDC 0054-0508

Generic Name
Icosapent Ethyl
Dosage Form
Capsule
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

Humco Holding Group, Inc.

NDC Product
Human Otc Drug

Humco Iodides Tincture
NDC 0395-1207

Generic Name
Ethyl Alcohol
Dosage Form
Liquid
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

L. Perrigo Company

NDC Product
Human Otc Drug

Good Sense Ibuprofen
NDC 0113-0298

Generic Name
Ibuprofen
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Good Sense Ibuprofen
NDC 0113-4501

Generic Name
Ibuprofen
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Good Sense Arthritis Pain
NDC 0113-8175

Generic Name
Diclofenac Sodium
Dosage Form
Gel
Route
Topical
Marketing
ANDA
Active Listing

Merck Sharp & Dohme LLC

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

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

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

Mylan Pharmaceuticals Inc.

NDC Product
Human Prescription Drug

Dabigatran Etexilate
NDC 0378-0265

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

Dabigatran Etexilate
NDC 0378-0266

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

Divalproex Sodium
NDC 0378-0472

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

Divalproex Sodium
NDC 0378-0473

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

Prazosin Hydrochloride
NDC 0378-1101

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

Mesalamine
NDC 0378-1375

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

Prazosin Hydrochloride
NDC 0378-2302

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

Esomeprazole Magnesium
NDC 0378-2350

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

Esomeprazole Magnesium
NDC 0378-2351

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

Prazosin Hydrochloride
NDC 0378-3205

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

Valacyclovir Hydrochloride
NDC 0378-4275

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

Valacyclovir Hydrochloride
NDC 0378-4276

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

Saxagliptin
NDC 0378-4705

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

Saxagliptin
NDC 0378-4706

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

Metformin Hydrochloride
NDC 0378-6001

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

Metformin Hydrochloride
NDC 0378-6002

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

Verapamil Hydrochloride
NDC 0378-6320

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

Acamprosate Calcium
NDC 0378-6333

Generic Name
Acamprosate Calcium Enteric-coated
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Verapamil Hydrochloride
NDC 0378-6380

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

Verapamil Hydrochloride
NDC 0378-6440

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

Sunitinib Malate
NDC 0378-6678

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

Sunitinib Malate
NDC 0378-6679

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

Sunitinib Malate
NDC 0378-6680

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

Sunitinib Malate
NDC 0378-6681

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

Lisdexamfetamine Dimesylate
NDC 0378-6855

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

Lisdexamfetamine Dimesylate
NDC 0378-6856

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

Lisdexamfetamine Dimesylate
NDC 0378-6857

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

Lisdexamfetamine Dimesylate
NDC 0378-6858

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

Lisdexamfetamine Dimesylate
NDC 0378-6859

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

Lisdexamfetamine Dimesylate
NDC 0378-6860

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

Acitretin
NDC 0378-7020

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

Acitretin
NDC 0378-7023

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

Lansoprazole
NDC 0378-8015

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

Fluvastatin Sodium
NDC 0378-8020

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

Fluvastatin Sodium
NDC 0378-8021

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

Lansoprazole
NDC 0378-8030

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

Saxagliptin And Metformin
NDC 0378-8175

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

Saxagliptin And Metformin
NDC 0378-8176

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

Saxagliptin And Metformin
NDC 0378-8177

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

Ketoprofen
NDC 0378-8200

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

Cystagon
NDC 0378-9040

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

Cystagon
NDC 0378-9045

Generic Name
Cysteamine Bitartrate
Dosage Form
Capsule
Route
Oral
Marketing
NDA
Active Listing

Novartis Pharmaceuticals Corporation

NDC Product
Human Prescription Drug

Fabhalta
NDC 0078-1189

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

Par Health USA, LLC

NDC Product
Human Prescription Drug

Alvimopan
NDC 0254-3012

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

Pfizer Laboratories Div Pfizer Inc

NDC Product
Human Prescription Drug

Ibrance
NDC 0069-0187

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

Ibrance
NDC 0069-0188

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

Ibrance
NDC 0069-0189

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

Xeljanz Xr
NDC 0069-0501

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

Xeljanz Xr
NDC 0069-0502

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

Xeljanz
NDC 0069-1002

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

Xeljanz
NDC 0069-1029

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

Xalkori
NDC 0069-8140

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

Xalkori
NDC 0069-8141

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

Vyndamax
NDC 0069-8730

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

SpecGx LLC

Teva Pharmaceuticals USA, Inc.

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

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

Mexiletine Hydrochloride
NDC 0093-8739

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

NDC 0093-8739

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

NDC 0093-8740

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

Mexiletine Hydrochloride
NDC 0093-8740

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

Mexiletine Hydrochloride
NDC 0093-8741

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

NDC 0093-8741

Generic Name
Mexiletine Hydrochloride
Dosage Form
Capsule
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing

Teva Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Lenalidomide
NDC 0480-1242

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

Lenalidomide
NDC 0480-1243

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

Lenalidomide
NDC 0480-1244

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

Lenalidomide
NDC 0480-1246

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

NDC 0480-2299

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

Phentermine And Topiramate
NDC 0480-2299

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

Topiramate
NDC 0480-2359

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

NDC 0480-2359

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

NDC 0480-3295

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

Phentermine And Topiramate
NDC 0480-3295

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

Phentermine And Topiramate
NDC 0480-3296

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

NDC 0480-3296

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

NDC 0480-3297

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

Phentermine And Topiramate
NDC 0480-3297

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

Gabapentin
NDC 0480-3494

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

NDC 0480-3494

Generic Name
Gabapentin
Dosage Form
Capsule
Route
N/A
Marketing
DRUG FOR FURTHER PROCESSING
Active Listing

WALGREEN CO.

NDC Product
Human Otc Drug

Esomeprazole Magnesium
NDC 0363-0508

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

Acetaminophen
NDC 0363-9798

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

Acetaminophen Diphenhydramine Hcl
NDC 0363-9799

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

WALGREENS

NDC Product
Human Otc Drug

Ibuprofen
NDC 0363-1610

Generic Name
Ibuprofen
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Ibuprofen
NDC 0363-8574

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

WALGREENS CO.

Walgreen Company

NDC Product
Human Otc Drug

Gentle Laxative
NDC 0363-0327

Generic Name
Bisacodyl
Dosage Form
Tablet, Delayed Release
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Wal-zyr D
NDC 0363-0989

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

Arthritis Pain Relieving
NDC 0363-3003

Generic Name
Diclofenac Sodium
Dosage Form
Gel
Route
Topical
Marketing
ANDA
Active Listing
NDC Product
Human Otc Drug

Arthritis Pain Relieving
NDC 0363-5123

Generic Name
Diclofenac Sodium
Dosage Form
Gel
Route
Topical
Marketing
ANDA
Active Listing

Walgreens

NDC Product
Human Otc Drug

Stool Softener Laxative
NDC 0363-4100

Generic Name
Docusate Sodium
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Stool Softener Laxative
NDC 0363-4202

Generic Name
Docusate Sodium
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Fexofenadine Hcl
NDC 0363-6231

Generic Name
Fexofenadine Hcl
Dosage Form
Tablet
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
NDC Product
Human Otc Drug

Diclofenac Sodium Topical Gel 1%
NDC 0363-7065

Generic Name
Diclofenac Sodium Topical Gel, 1%
Dosage Form
Gel
Route
Topical
Marketing
ANDA
Active Listing

External Clinical & Regulatory Resources

CAS
Common Chemistry
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NLM
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