FRUCTOSE
UNII 6YSS42VSEV

Substance Identification & Data

This profile provides standardized clinical and technical data for Fructose, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 6YSS42VSEV.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 57-48-7 and the RxNorm Concept ID (RxCUI) 4570. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
6YSS42VSEV
CAS Registry Number
57-48-7
RxNorm Concept ID
4570

Detailed Substance Profile

Preferred Name
FRUCTOSE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
6YSS42VSEV
The specific atomic composition represented as a molecular structure string.
InChIKey
C6H12O6
International Chemical Identifier digital signature for unique molecular identification.
SMILES String
BJHIKXHVCXFQLS-UYFOZJQFSA-N
Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
C68480
National Cancer Institute reference terminology for clinical and research data.
PubChem CID
5984
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@H]([C@@H](C(CO)=O)O)([C@@H](CO)O)O

Synonyms and Nomenclature

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

FRUCTOSE

Common Names & Synonyms

D-FRUCTOSE
FRUCTOSE (CONSTITUENT OF CRANBERRY LIQUID PREPARATION) [DSC]
FRUCTOSE [EP IMPURITY]
FRUCTOSE [EP MONOGRAPH]
FRUCTOSE [FCC]
FRUCTOSE [II]
FRUCTOSE [JAN]
FRUCTOSE [MART.]
FRUCTOSE [MI]
FRUCTOSE [USP MONOGRAPH]
FRUCTOSE [USP-RS]
FRUCTOSE [WHO-DD]
GLUCOSE IMPURITY D [EP IMPURITY]
LACTULOSE IMPURITY D [EP IMPURITY]
LEVULOSE
NEVULOSE
SUGAR FRUIT FINE
SUGAR FRUIT FINE [II]
TOPIRAMATE IMPURITY, FRUCTOSE- [USP IMPURITY]

Systematic Nomenclature

D-ARABINO-HEX-2-ULOPYRANOSE

Technical Codes

NSC-760385
NSC-9250

NDC Products Containing FRUCTOSE

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 (292), only Active Listings are currently displayed.
→ AMERISOURCE BERGEN 1
→ ANI Pharmaceuticals, Inc. 3
→ ATLANTIC BIOLOGICALS CORP. 1
→ Access Business Group LLC 1
→ Actavis Pharma, Inc. 2
→ Allure Labs 7
→ Amneal Pharmaceuticals LLC 3
→ Amneal Pharmaceuticals NY LLC 1
→ Apotex Corp. 1
→ Ascend Laboratories, LLC 2
→ Atlantic Biologicals Corps 1
→ Aurobindo Pharma Limited 1
→ Avion Pharmaceuticals, LLC 1
→ BEST CHOICE (VALU MERCHANDISERS COMPANY) 1
→ BURT'S BEES, INC. 1
→ BioActive Nutritional, Inc. 1
→ Biological M.D. Solutions LLC 2
→ Bluemercury 1
→ Bryant Ranch Prepack 8
→ COLGATE PALMOLIVE COMPANY 1
→ CONTROL CORRECTIVE SKINCARE INC 1
→ COSMAX USA, CORPORATION 1
→ CVS PHARMACY 1
→ CVS PHARMACY,INC. 1
→ Camber Pharmaceuticals, Inc. 1
→ Cardinal Health 1
→ Chartwell RX, LLC 3
→ CosMedical Technologies, LLC 1
→ Crown Laboratories, Inc. 1
→ DISCOUNT DRUG MART 1
→ Dr. Donna Restivo DC 1
→ Dr. Loretta, LLC 1
→ Dr.Reddy's Laboratories Inc., 2
→ EPIC PHARMA, LLC 6
→ Energique, Inc. 1
→ Exeltis USA, Inc. 1
→ FH2 Pharma LLC 1
→ Forte Bio-Pharma LLC 1
→ Golden State Medical Supply, Inc. 2
→ Guangdong Bisutang Biotechnology Co., LTD 1
→ Guna spa 1
→ HEB 1
→ Hikma Pharmaceuticals USA Inc. 5
→ I World Pharmaceutical Co., Ltd. 2
→ Industria La Popular, S.A. 2
→ KROGER COMPANY 1
→ Kao USA Inc. 1
→ Kobayashi Healthcare International, Inc. 2
→ LABORATOIRES DRUIDE INC 1
→ MEIJER DISTRIBUTION, INC. 1
→ Macleods Pharmaceuticals Limited 2
→ MediNatura 1
→ Merck Sharp & Dohme LLC 4
→ Micro Labs Limited 1
→ NaturalCare 1
→ Neos Therapeutics Brands, LLC 9
→ Neos Therapeutics, LP 6
→ NorthStar RxLLC 1
→ Norwex Usa, Inc. 1
→ PAI Holdings, LLC dba PAI Pharma 1
→ PHARMACY VALUE ALLIANCE, LLC 1
→ PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS 3
→ Pharmadel LLC 1
→ Plexus Worldwide, LLC 1
→ Professional Complementary Health Formulas 1
→ PureTek Corporation 5
→ Puretek Corporation 2
→ QUAGEN PHARMACEUTICALS LLC 1
→ QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION) 3
→ REVLON 1
→ RUGBY LABORATORIES 1
→ Revlon Consumer Products Corp 1
→ Roerig 3
→ SOLARA SUNCARE, INC. 5
→ Schwabe North America, Inc 4
→ Schwabe North America, Inc. 1
→ Shenzhen Zealous Ecommerce Technology Co., Ltd 4
→ THE PROCTER & GAMBLE MANUFACTURING COMPANY 1
→ TOPCO ASSOCIATES LLC 1
→ Teva Women's Health, Inc. 1
→ The Procter & Gamble Manufacturing Company 3
→ VistaPharm, LLC 1
→ WALGREENS CO. 3
→ WellSpring Pharmaceutical Corporation 5

AMERISOURCE BERGEN

NDC Product
Human Otc Drug

Good Neighbor Anti Nausea Cherry Flavor
NDC 46122-729

Generic Name
Dextrose(glucose),levulose(fructose),phosphoric Acid
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

ANI Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Tadalafil
NDC 70954-433

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

Tadalafil
NDC 70954-434

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

Tadalafil
NDC 70954-435

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

ATLANTIC BIOLOGICALS CORP.

NDC Product
Human Prescription Drug

Aripiprazole
NDC 17856-0684

Generic Name
Aripiprazole Oral
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

Access Business Group LLC

NDC Product
Human Otc Drug

G And H Protect Body
NDC 10056-025

Generic Name
Ensulizole, Octisalate, Zinc Oxide
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Actavis Pharma, Inc.

NDC Product
Human Prescription Drug

Enulose
NDC 45963-438

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

Constulose
NDC 45963-439

Generic Name
Lactulose
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

Allure Labs

NDC Product
Human Otc Drug

Bb Tint 30 Bs Spf 30
NDC 62742-4246

Generic Name
Zinc Oxide And Titanium Dioxide
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Bb Brite 30 Bs Spf30
NDC 62742-4247

Generic Name
Zinc Oxide And Titanium Dioxide
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Bb Bronze 30 Bs Spf30
NDC 62742-4248

Generic Name
Zinc Oxide And Titanium Dioxide
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Bb Noir 30 Bs Spf30
NDC 62742-4249

Generic Name
Zinc Oxide And Titanium Dioxide
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Bb Blanc 30 Bs Spf30
NDC 62742-4250

Generic Name
Zinc Oxide And Titanium Dioxide
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Bb Sienna 30 Bs Spf30
NDC 62742-4251

Generic Name
Zinc Oxide And Titanium Dioxide
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Bb Ambre 30 Bs Spf30
NDC 62742-4252

Generic Name
Zinc Oxide And Titanium Dioxide
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Amneal Pharmaceuticals LLC

NDC Product
Human Prescription Drug

Fesoterodine Fumarate
NDC 65162-369

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

Fesoterodine Fumarate
NDC 65162-370

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

Aripiprazole
NDC 65162-893

Generic Name
Aripiprazole
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

Amneal Pharmaceuticals NY LLC

NDC Product
Human Prescription Drug

Prednisolone Sodium Phosphate
NDC 69238-2122

Generic Name
Prednisolone Sodium Phosphate
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

Apotex Corp.

NDC Product
Human Prescription Drug

Aripiprazole
NDC 60505-0404

Generic Name
Aripiprazole
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

Ascend Laboratories, LLC

NDC Product
Human Prescription Drug

Cholestyramine Powder For Suspension
NDC 67877-298

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

Choleystyramine Light
NDC 67877-422

Generic Name
Choleystyramine Light
Dosage Form
Powder, For Suspension
Route
Oral
Marketing
ANDA
Active Listing

Atlantic Biologicals Corps

NDC Product
Human Prescription Drug

Prednisone
NDC 17856-3722

Generic Name
Prednisone
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

Aurobindo Pharma Limited

NDC Product
Human Prescription Drug

Aripiprazole
NDC 59651-110

Generic Name
Aripiprazole
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

Avion Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Prenate Chewable
NDC 75854-306

Generic Name
Calcium Carbonate, Cholecalciferol, Magnesium Oxide, Boron, ...
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

BEST CHOICE (VALU MERCHANDISERS COMPANY)

NDC Product
Human Otc Drug

Best Choice Anti Nausea Cherry Flavor
NDC 63941-708

Generic Name
Dextrose(glucose),levulose(fructose),phosphoric Acid
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

BURT'S BEES, INC.

NDC Product
Human Otc Drug

Nas Toner
NDC 26052-042

Generic Name
Salicylic Acid
Dosage Form
Liquid
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

BioActive Nutritional, Inc.

NDC Product
Human Otc Drug

Energizer
NDC 43857-0346

Generic Name
Phosphoricum Acidum, Cocculus Indicus, Helonias Dioica, Igna...
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Biological M.D. Solutions LLC

NDC Product
Human Otc Drug

Med O-3 Bio-
NDC 83538-101

Generic Name
Methyl Salicylate, Menthol, Capsaicin
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Oprava
NDC 83538-102

Generic Name
Methyl Salicylate, Menthol, Capsaicin
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Bluemercury

NDC Product
Human Otc Drug

Hydraboost Moisturizer Spf 30
NDC 72203-001

Generic Name
Avobenzone, Homosalate, Octisalate, And Octocrylene
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Bryant Ranch Prepack

NDC Product
Human Prescription Drug

Enulose
NDC 63629-8800

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

Cholestyramine Powder For Suspension
NDC 63629-9196

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

Choleystyramine Light
NDC 63629-9466

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

Cholestyramine Powder For Suspension
NDC 71335-2902

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

Cholestyramine Powder For Suspension
NDC 72162-1834

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

Multi-vit-flor
NDC 72162-2272

Generic Name
Sodium Fluoride, Vitamin A Acetate, Sodium Ascorbate, Cholec...
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Multi-vit-flor
NDC 72162-2273

Generic Name
Sodium Fluoride, Vitamin A Acetate, Sodium Ascorbate, Cholec...
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Multi-vit-flor
NDC 72162-2274

Generic Name
Sodium Fluoride, Vitamin A Acetate, Sodium Ascorbate, Cholec...
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

COLGATE PALMOLIVE COMPANY

CONTROL CORRECTIVE SKINCARE INC

NDC Product
Human Otc Drug

Acne Spot Treatment
NDC 70764-105

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

COSMAX USA, CORPORATION

CVS PHARMACY

NDC Product
Human Otc Drug

Cvs Anti Nausea Cherry Flavor
NDC 69842-708

Generic Name
Dextrose(glucose),levulose(fructose),phosphoric Acid
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

CVS PHARMACY,INC.

NDC Product
Human Otc Drug

Cvs Health Nausea Relief
NDC 69842-423

Generic Name
Sodium Citrate Dihydrate
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Camber Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Aripiprazole
NDC 31722-684

Generic Name
Aripiprazole Oral
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

Cardinal Health

NDC Product
Human Otc Drug

Anti Nausea
NDC 70000-0052

Generic Name
Dextrose(glucose),levulose(fructose),phosphoric Acid
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Chartwell RX, LLC

NDC Product
Human Prescription Drug

Cholestyramine For Oral Suspension
NDC 62135-008

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

Aripiprazole
NDC 62135-904

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

Cholestyramine For Oral Suspension
NDC 62135-937

Generic Name
Cholestyramine For Oral Suspension
Dosage Form
Powder
Route
Oral
Marketing
ANDA
Active Listing

CosMedical Technologies, LLC

NDC Product
Human Otc Drug

Ultra Replenishing Sunscreen Spf 40
NDC 70060-1901

Generic Name
Homosalate, Octisalate, Octocrylene, Zinc Oxyide Cream
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Crown Laboratories, Inc.

NDC Product
Human Otc Drug

Sarna
NDC 0316-0256

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

DISCOUNT DRUG MART

Dr. Donna Restivo DC

NDC Product
Human Otc Drug

Sugar Cravings
NDC 62185-0057

Generic Name
Cinnamic Acid, Phloridzinum, Argentum Nitricum, Adenosinum T...
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Dr. Loretta, LLC

NDC Product
Human Otc Drug

Urban Antioxidant Sunscreen Spf 40
NDC 71501-1902

Generic Name
Homosalate, Octisalate, Octocrylene, Zinc Oxyide Cream
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Dr.Reddy's Laboratories Inc.,

NDC Product
Human Prescription Drug

Fesoterodine Fumarate
NDC 43598-247

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

Fesoterodine Fumarate
NDC 43598-248

Generic Name
Fesoterodine Fumarate
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

EPIC PHARMA, LLC

NDC Product
Human Prescription Drug

Cholestyramine
NDC 42806-265

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

Cholestyramine
NDC 42806-266

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

Cholestyramine
NDC 42806-267

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

Cholestyramine Light
NDC 42806-269

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

Cholestyramine Light
NDC 42806-270

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

Cholestyramine Light
NDC 42806-271

Generic Name
Cholestyramine Light
Dosage Form
Powder, For Suspension
Route
Oral
Marketing
ANDA
Active Listing

Energique, Inc.

NDC Product
Human Otc Drug

Liquid B
NDC 44911-0502

Generic Name
Hordeum Vulgare, Hepar Suis, Heart (suis), Torula Cerevisiae
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Exeltis USA, Inc.

NDC Product
Human Prescription Drug

Select-ob Plus Dha Prenatal Supplement Plus Dha
NDC 0642-0075

Generic Name
.beta.-carotene, Vitamin A Acetate, Ascorbic Acid, Cholecalc...
Dosage Form
Kit
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Active Listing

FH2 Pharma LLC

Forte Bio-Pharma LLC

NDC Product
Human Prescription Drug

Prolate
NDC 72245-648

Generic Name
Oxycodone Hydrochloride And Acetaminophen
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

Golden State Medical Supply, Inc.

NDC Product
Human Prescription Drug

Fesoterodine Fumarate
NDC 51407-661

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

Fesoterodine Fumarate
NDC 51407-662

Generic Name
Fesoterodine Fumarate
Dosage Form
Tablet, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Guangdong Bisutang Biotechnology Co., LTD

NDC Product
Human Otc Drug

Magnet Eye Sheet Mask
NDC 84753-039

Generic Name
Eye Mask
Dosage Form
Patch
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Guna spa

NDC Product
Human Otc Drug

Guna-cough
NDC 17089-453

Generic Name
Althaea Officinalis Leaf - Antimony Potassium Tartrate - Bry...
Dosage Form
Solution/ Drops
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

HEB

NDC Product
Human Otc Drug

Heb Anti Nausea
NDC 37808-883

Generic Name
Dextrose(glucose),levulose(fructose),phosphoric Acid
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Hikma Pharmaceuticals USA Inc.

NDC Product
Human Prescription Drug

Prednisone Intensol
NDC 0054-3721

Generic Name
Prednisone Intensol
Dosage Form
Solution, Concentrate
Route
Oral
Marketing
ANDA
Active Listing
NDC Product
Human Prescription Drug

Prednisone
NDC 0054-3722

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

Prednisone
NDC 0054-8724

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

Prednisone
NDC 0054-8739

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

Prednisone
NDC 0054-8740

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

I World Pharmaceutical Co., Ltd.

NDC Product
Human Otc Drug

Ssangbi Tang
NDC 73442-0008

Generic Name
Galgeun-tang Extract
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc Drug

Ssanggi Tang
NDC 73442-0009

Generic Name
Ssanghwa Extract
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Industria La Popular, S.A.

NDC Product
Human Otc Drug

Dk12 Shower Gel Creamy
NDC 62476-010

Generic Name
Benzalkonium Chloride 0.13%
Dosage Form
Gel
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Dk12 Shower Gel Fresh Energy
NDC 62476-011

Generic Name
Benzalkonium Chloride 0.13%
Dosage Form
Gel
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

KROGER COMPANY

NDC Product
Human Otc Drug

Kroger Anti Nausea Cherry Flavor
NDC 30142-708

Generic Name
Dextrose(glucose),levulose(fructose),phosphoric Acid
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Kao USA Inc.

Kobayashi Healthcare International, Inc.

NDC Product
Human Otc Drug

Nauzene
NDC 52389-242

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

Nauzene Chewables Ginger Honey
NDC 52389-677

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

LABORATOIRES DRUIDE INC

MEIJER DISTRIBUTION, INC.

NDC Product
Human Otc Drug

Meijer Anti Nausea
NDC 41250-495

Generic Name
Dextrose(glucose),levulose(fructose),phosphoric Acid
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Macleods Pharmaceuticals Limited

NDC Product
Human Prescription Drug

Cholestyramine
NDC 33342-293

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

Cholestyramine
NDC 33342-319

Generic Name
Cholestyramine
Dosage Form
Powder, For Suspension
Route
Oral
Marketing
ANDA
Active Listing

MediNatura

NDC Product
Human Otc Drug

Reboost
NDC 62795-4004

Generic Name
Apis Mellifera, Atropa Belladonna, Zinc Gluconate, Baptisia ...
Dosage Form
Spray
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
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

Micro Labs Limited

NDC Product
Human Prescription Drug

Cholestyramine
NDC 42571-508

Generic Name
Cholestyramine
Dosage Form
Powder, For Suspension
Route
Oral
Marketing
ANDA
Active Listing

NaturalCare

NDC Product
Human Otc Drug

Sore Throat
NDC 70163-0200

Generic Name
Capsicum Annuum, Echinacea (angustifolia), Eucalyptus Globul...
Dosage Form
Spray
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Neos Therapeutics Brands, LLC

NDC Product
Human Prescription Drug

Adzenys Xr-odt
NDC 70165-005

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

Adzenys Xr-odt
NDC 70165-010

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

Adzenys Xr-odt
NDC 70165-015

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

Adzenys Xr-odt
NDC 70165-020

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

Adzenys Xr-odt
NDC 70165-025

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

Adzenys Xr-odt
NDC 70165-030

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

Cotempla Xr-odt
NDC 70165-100

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

Cotempla Xr-odt
NDC 70165-200

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

Cotempla Xr-odt
NDC 70165-300

Generic Name
Methylphenidate
Dosage Form
Tablet, Orally Disintegrating
Route
Oral
Marketing
NDA
Active Listing

Neos Therapeutics, LP

NDC Product
Human Prescription Drug

Amphetamine Extended-release
NDC 62542-005

Generic Name
Amphetamine Extended-release
Dosage Form
Tablet, Orally Disintegrating
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Amphetamine Extended-release
NDC 62542-010

Generic Name
Amphetamine Extended-release
Dosage Form
Tablet, Orally Disintegrating
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Amphetamine Extended-release
NDC 62542-015

Generic Name
Amphetamine Extended-release
Dosage Form
Tablet, Orally Disintegrating
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Amphetamine Extended-release
NDC 62542-020

Generic Name
Amphetamine Extended-release
Dosage Form
Tablet, Orally Disintegrating
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Amphetamine Extended-release
NDC 62542-025

Generic Name
Amphetamine Extended-release
Dosage Form
Tablet, Orally Disintegrating
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription Drug

Amphetamine Extended-release
NDC 62542-030

Generic Name
Amphetamine Extended-release
Dosage Form
Tablet, Orally Disintegrating
Route
Oral
Marketing
NDA AUTHORIZED GENERIC
Active Listing

NorthStar RxLLC

NDC Product
Human Prescription Drug

Aripiprazole
NDC 72603-445

Generic Name
Aripiprazole Oral
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

Norwex Usa, Inc.

PAI Holdings, LLC dba PAI Pharma

NDC Product
Human Prescription Drug

Ondansetron
NDC 0121-0882

Generic Name
Ondansetron
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

PHARMACY VALUE ALLIANCE, LLC

NDC Product
Human Otc Drug

Premier Value Nausea Control Cherry Flavor
NDC 68016-807

Generic Name
Dextrose(glucose),levulose(fructose),phosphoric Acid
Dosage Form
Solution
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS

NDC Product
Human Prescription Drug

Cholestyramine
NDC 24658-266

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

Cholestyramine Light
NDC 24658-270

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

Cholestyramine Light
NDC 24658-271

Generic Name
Cholestyramine Light
Dosage Form
Powder, For Suspension
Route
Oral
Marketing
ANDA
Active Listing

Pharmadel LLC

NDC Product
Human Otc Drug

Vitapirena
NDC 55758-012

Generic Name
Acetaminophen
Dosage Form
Granule, For Solution
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Plexus Worldwide, LLC

Professional Complementary Health Formulas

NDC Product
Human Otc Drug

Glucose Drops 2031
NDC 63083-2031

Generic Name
Glucose Drops
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

PureTek Corporation

NDC Product
Human Otc Drug

Menticam
NDC 59088-202

Generic Name
Camphor,menthol, Methyl Salicylate
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Mencylate Pain Relieving
NDC 59088-215

Generic Name
Menthol, Methyl Salicylate
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Methylten 25% Pain Relieving
NDC 59088-245

Generic Name
Methyl Salicylate
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Capasil Pain Relieving
NDC 59088-434

Generic Name
Menthol, Methyl Salicylate
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Puretek Corporation

NDC Product
Human Otc Drug

Methylten
NDC 59088-013

Generic Name
Methyl Salicylate 10%
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

QUAGEN PHARMACEUTICALS LLC

NDC Product
Human Prescription Drug

Aripiprazole
NDC 70752-114

Generic Name
Aripiprazole
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)

NDC Product
Human Otc Drug

Anti Nausea Liquid Cherry Flavor
NDC 63868-704

Generic Name
Dextrose(glucose),levulose(fructose),phosphoric Acid
Dosage Form
Solution
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc Drug

Quality Choice Anti-nausea
NDC 83324-217

Generic Name
Dextrose(glucose),levulose(fructose),phosphoric Acid
Dosage Form
Solution
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc Drug

Quality Choice Nausea Relief
NDC 83324-300

Generic Name
Sodium Citrate Dihydrate
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

REVLON

NDC Product
Human Otc Drug

Ceramide Makeup Spf 15
NDC 10967-668

Generic Name
Octinoxate, Titanium Dioxide
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

RUGBY LABORATORIES

NDC Product
Human Otc Drug

Anti Nausea
NDC 0536-1302

Generic Name
Dextrose(glucose),levulose(fructose),phosphoric Acid
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Revlon Consumer Products Corp

Roerig

NDC Product
Human Prescription Drug

Eraxis
NDC 0049-0114

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

Eraxis
NDC 0049-0116

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

Eraxis
NDC 0049-2242

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

SOLARA SUNCARE, INC.

Schwabe North America, Inc

NDC Product
Human Otc Drug

Cold Relief Syrup Kids Cherry
NDC 53499-1165

Generic Name
Pelargonium Sidoides
Dosage Form
Syrup
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc Drug

Cold Relief Menthol
NDC 53499-6272

Generic Name
Pelargonium Sidoides
Dosage Form
Syrup
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc Drug

Cold Relief Syrup Cherry
NDC 53499-6273

Generic Name
Pelargonium Sidoides
Dosage Form
Syrup
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc Drug

Viraclear Eps 7630 Cherry Flavor
NDC 59800-8002

Generic Name
Pelargonium Sidoides
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Schwabe North America, Inc.

NDC Product
Human Otc Drug

Sambucus Flu Relief
NDC 53499-0803

Generic Name
Aconitum Napellus, Bryonia Alba Root, Eucalyptus Globulus Le...
Dosage Form
Syrup
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Shenzhen Zealous Ecommerce Technology Co., Ltd

NDC Product
Human Otc Drug

Qanskm Bee Venom Skin Cream
NDC 85587-002

Generic Name
Skin Cream
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Jitagix Bee Venom Skin Cream
NDC 85587-006

Generic Name
Skin Cream
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Neatique Bee Venom Skin Cream
NDC 85587-007

Generic Name
Skin Cream
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

THE PROCTER & GAMBLE MANUFACTURING COMPANY

TOPCO ASSOCIATES LLC

NDC Product
Human Otc Drug

Anti Nausea Liquid
NDC 36800-708

Generic Name
Phosphorated Carbohydrate
Dosage Form
Solution
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Teva Women's Health, Inc.

The Procter & Gamble Manufacturing Company

VistaPharm, LLC

NDC Product
Human Prescription Drug

Aripiprazole
NDC 66689-735

Generic Name
Aripiprazole
Dosage Form
Solution
Route
Oral
Marketing
ANDA
Active Listing

WALGREENS CO.

NDC Product
Human Otc Drug

Walgreen Anti Nausea Cherry Flavor
NDC 0363-7080

Generic Name
Phosphorated Carbohydrate
Dosage Form
Solution
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc Drug

Walgreen Children Anti Nausea
NDC 0363-7081

Generic Name
Dextrose, Levulose, Phosphoric Acid
Dosage Form
Solution
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

WellSpring Pharmaceutical Corporation

NDC Product
Human Otc Drug

Emetrol Cherry
NDC 65197-201

Generic Name
Phosphorated Carbohydrate
Dosage Form
Solution
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc Drug

Emetrol Children Mixed Berry
NDC 65197-202

Generic Name
Phosphorated Carbohydrate
Dosage Form
Solution
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc Drug

Emetrol Chewables
NDC 65197-204

Generic Name
Sodium Citrate Dihydrate
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc Drug

Emetrol Chewables Orange
NDC 65197-410

Generic Name
Sodium Citrate Dihydrate
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc Drug

Emetrol Chewables Mixed Berry
NDC 65197-420

Generic Name
Sodium Citrate Dihydrate
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

External Clinical & Regulatory Resources

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