POLYDEXTROSE
UNII VH2XOU12IE

Substance Identification & Data

This profile provides standardized clinical and technical data for Polydextrose, uniquely identified by the FDA Unique Ingredient Identifier (UNII) VH2XOU12IE.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 68424-04-4 and the RxNorm Concept ID (RxCUI) 1363053. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
VH2XOU12IE
CAS Registry Number
68424-04-4
RxNorm Concept ID
1363053

Detailed Substance Profile

Preferred Name
POLYDEXTROSE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
VH2XOU12IE
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
C81624
National Cancer Institute reference terminology for clinical and research data.
Substance Type
polymer
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).

Synonyms and Nomenclature

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

POLYDEXTROSE

Common Names & Synonyms

D-GLUCOSE POLYMER, REACTION PRODUCT WITH CITRIC ACID AND SORBITOL
E1200
LITESSE III SYRUP
MODIFIED POLYDEXTROSES
POLYDEXTROSE [FCC]
POLYDEXTROSE [II]
POLYDEXTROSE [MI]
POLYDEXTROSE [USAN]
POLYDEXTROSE [USP-RS]
POLYDEXTROSE [VANDF]
POLYDEXTROSE [WHO-DD]
POLYDEXTROSE A
POLYDEXTROSE F
POLYDEXTROSE SOLUTION
POLYDEXTROSE SOLUTION [FCC]
POLYDEXTROSE-K
POLYDEXTROSES-1200

Brand / Trade Names

LITESSE
LITESSE ULTRA
STA-LITE

Technical Codes

CP-31,081
CP-31081
E-1200
INS NO.1200
INS-1200

NDC Products Containing POLYDEXTROSE

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.
→ Acme United Corporation 1
→ Actavis Pharma, Inc. 9
→ Amneal Pharmaceuticals of New York LLC 10
→ AstraZeneca Pharmaceuticals LP 2
→ Bausch Health US LLC 8
→ Beach Products, Inc. 1
→ C.B. Fleet Company, Inc. 1
→ Church & Dwight Co., Inc. 1
→ Exeltis USA, Inc 1
→ Exeltis USA, Inc. 1
→ Haleon US Holdings LLC 10
→ Henry Schein Inc. 1
→ Hikma Pharmaceuticals USA Inc 3
→ Hikma Pharmaceuticals USA Inc. 3
→ L. Perrigo Company 2
→ MAJOR PHARMACEUTICALS 1
→ Major Pharmaceuticals 11
→ Marlex Pharmaceuticals Inc 2
→ Marlex Pharmaceuticals, Inc. 1
→ Mission Pharmacal Company 2
→ Mylan Pharmaceuticals Inc. 53
→ NCS HealthCare of KY, LLC dba Vangard Labs 5
→ RITE AID 1
→ RUGBY LABORATORIES 1
→ Rite Aid Corporation 9
→ Rugby Laboratories 3
→ SpecGx LLC 5
→ TARGET CORPORATION 1
→ Target Corporation 2
→ Teva Pharmaceuticals USA, Inc. 26
→ WALGREEN COMPANY 1
→ WALGREENS 1
→ Walgreen Company 20
→ Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. 1

Acme United Corporation

NDC Product
Human Otc Drug

Physicians Care Ibuprofen
NDC 0924-0075

Generic Name
Ibuprofen 200mg
Dosage Form
Tablet, Coated
Route
Oral
Marketing
ANDA
Active Listing

Actavis Pharma, Inc.

NDC Product
Human Prescription Drug

Lamotrigine
NDC 0228-1638

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

NDC 0228-2571

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

Indapamide
NDC 0228-2571

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

Indapamide
NDC 0228-2597

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

NDC 0228-2597

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

Ropinirole
NDC 0228-3640

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

Ropinirole
NDC 0228-3659

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

Ropinirole
NDC 0228-3660

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

Ropinirole
NDC 0228-3661

Generic Name
Ropinirole
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing
ANDA
Active Listing

Amneal Pharmaceuticals of New York LLC

NDC Product
Human Prescription Drug

Bupropion Hydrochloride
NDC 0115-5445

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

Fenofibrate
NDC 0115-5511

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

Fenofibrate
NDC 0115-5522

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

Bupropion Hydrochloride
NDC 0115-6811

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

AstraZeneca Pharmaceuticals LP

NDC Product
Human Prescription Drug

Truqap
NDC 0310-9500

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

Truqap
NDC 0310-9501

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

Bausch Health US LLC

NDC Product
Human Prescription Drug

Cardizem La
NDC 0187-2045

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

Cardizem La
NDC 0187-2046

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

Cardizem La
NDC 0187-2047

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

Cardizem La
NDC 0187-2048

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

Cardizem La
NDC 0187-2049

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

Cardizem La
NDC 0187-2050

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

Pepcid
NDC 0187-4420

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

Pepcid
NDC 0187-4440

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

Beach Products, Inc.

NDC Product
Human Prescription Drug

K-phos No. 2
NDC 0486-1134

Generic Name
Potassium Phosphate, Monobasic And Sodium Phosphate, Monobas...
Dosage Form
Tablet, Coated
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
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

Church & Dwight Co., Inc.

Exeltis USA, Inc

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

Haleon US Holdings LLC

NDC Product
Human Otc Drug

Excedrin Pm Triple Action Caplets
NDC 0067-2056

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

Advil Pm
NDC 0573-0164

Generic Name
Diphenhydramine Citrate And Ibuprofen
Dosage Form
Tablet, Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Otc Drug

Advil Allergy Sinus
NDC 0573-0188

Generic Name
Chlorpheniramine Maleate, Ibuprofen, Pseudoephedrine Hcl
Dosage Form
Tablet, Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Otc Drug

Advil Multi-symptom Cold And Flu
NDC 0573-0190

Generic Name
Chlorpheniramine Maleate, Ibuprofen, Phenylephrine Hcl
Dosage Form
Tablet, Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Otc Drug

Advil Allergy And Congestion Relief
NDC 0573-0196

Generic Name
Chlorpheniramine Maleate, Ibuprofen, And Phenylephrine Hydro...
Dosage Form
Tablet, Coated
Route
Oral
Marketing
NDA
Active Listing
NDC Product
Human Otc Drug

Advil Sinus Congestion And Pain
NDC 0573-0199

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

Henry Schein Inc.

NDC Product
Human Otc Drug

Henry Schein Ibuprofen
NDC 0404-0017

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

Hikma Pharmaceuticals USA Inc

NDC Product
Human Prescription Drug

Prucalopride
NDC 0054-0749

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

Prucalopride
NDC 0054-0750

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

Combogesic
NDC 0143-9432

Generic Name
Acetaminophen And Ibuprofen
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
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

Galantamine Hydrobromide
NDC 0054-0137

Generic Name
Galantamine Hydrobromide
Dosage Form
Solution
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

L. Perrigo Company

NDC Product
Human Otc Drug

Good Sense Acid Reducer
NDC 0113-0141

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

Good Sense All Day Allergy
NDC 0113-9458

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

MAJOR PHARMACEUTICALS

NDC Product
Human Otc Drug

Aspirin Low Dose
NDC 0904-6783

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

Major Pharmaceuticals

NDC Product
Human Otc Drug

Sudogest
NDC 0904-5053

Generic Name
Pseudoephedrine Hcl
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Bisacodyl
NDC 0904-6407

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

Cetirizine
NDC 0904-6717

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

Bisacodyl
NDC 0904-6748

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

Aspirin Low Dose
NDC 0904-6751

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

Ursodiol
NDC 0904-6890

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

Pseudoephedrine Hcl
NDC 0904-6990

Generic Name
Pseudoephedrine Hcl
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Prescription Drug

Colchicine
NDC 0904-7120

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

Cetirizine
NDC 0904-7510

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

Ibuprofen
NDC 0904-7914

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

Marlex Pharmaceuticals Inc

NDC Product
Human Prescription Drug

Labetalol Hydrochloride
NDC 10135-712

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

Labetalol Hydrochloride
NDC 10135-713

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

Marlex Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Diclofenac Potassium
NDC 10135-806

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

Mission Pharmacal Company

NDC Product
Human Prescription Drug

Tindamax
NDC 0178-8250

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

Tindamax
NDC 0178-8500

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

Mylan Pharmaceuticals Inc.

NDC Product
Drug For Further Processing

NDC 0378-0018

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

Metoprolol Tartrate
NDC 0378-0018

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

Metoprolol Tartrate
NDC 0378-0032

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

NDC 0378-0032

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

NDC 0378-0047

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

Metoprolol Tartrate
NDC 0378-0047

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

Cimetidine
NDC 0378-0053

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

Spironolactone
NDC 0378-0243

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

Cimetidine
NDC 0378-0317

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

Cimetidine
NDC 0378-0372

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

Spironolactone
NDC 0378-0437

Generic Name
Spironolactone
Dosage Form
Tablet, Film Coated
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

Cimetidine
NDC 0378-0541

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

Colchicine
NDC 0378-1086

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

Ketorolac Tromethamine
NDC 0378-1134

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

Spironolactone
NDC 0378-2146

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

Trifluoperazine Hydrochloride
NDC 0378-2401

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

Trifluoperazine Hydrochloride
NDC 0378-2402

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

Trifluoperazine Hydrochloride
NDC 0378-2405

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

Trifluoperazine Hydrochloride
NDC 0378-2410

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

Mirtazapine
NDC 0378-3515

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

Mirtazapine
NDC 0378-3530

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

Mirtazapine
NDC 0378-3545

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

Cetirizine Hydrochloride
NDC 0378-3635

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

Cetirizine Hydrochloride
NDC 0378-3637

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

Budesonide
NDC 0378-4500

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

Metoprolol Tartrate
NDC 0378-4593

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

Metoprolol Tartrate
NDC 0378-4594

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

Levetiracetam
NDC 0378-5615

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

Levetiracetam
NDC 0378-5617

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

Levetiracetam
NDC 0378-5619

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

Sumatriptan Succinate
NDC 0378-5630

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

NDC 0378-5630

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

NDC 0378-5631

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

Sumatriptan Succinate
NDC 0378-5631

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

Sumatriptan Succinate
NDC 0378-5632

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

NDC 0378-5632

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

Citalopram
NDC 0378-6231

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

Citalopram
NDC 0378-6232

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

Citalopram
NDC 0378-6233

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

Valsartan And Hydrochlorothiazide
NDC 0378-6321

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

Valsartan And Hydrochlorothiazide
NDC 0378-6322

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

Valsartan And Hydrochlorothiazide
NDC 0378-6323

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

Valsartan And Hydrochlorothiazide
NDC 0378-6324

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

Valsartan And Hydrochlorothiazide
NDC 0378-6325

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

Paroxetine
NDC 0378-7001

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

Paroxetine
NDC 0378-7002

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

Paroxetine
NDC 0378-7003

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

Paroxetine
NDC 0378-7004

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

NCS HealthCare of KY, LLC dba Vangard Labs

NDC Product
Human Prescription Drug

Diltiazem Hydrochloride
NDC 0615-8379

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

Diltiazem Hydrochloride
NDC 0615-8380

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

Diltiazem Hydrochloride
NDC 0615-8381

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

Bupropion Hydrochloride
NDC 0615-8581

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

Bupropion Hydrochloride
NDC 0615-8582

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

RITE AID

NDC Product
Human Otc Drug

Acetaminophen And Ibuprofen (nsaid)
NDC 11822-1131

Generic Name
Acetaminophen And Ibuprofen (nsaid)
Dosage Form
Tablet
Route
Oral
Marketing
ANDA
Active Listing

RUGBY LABORATORIES

NDC Product
Human Otc Drug

Acetaminophen And Ibuprofen
NDC 0536-1376

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

Rite Aid Corporation

NDC Product
Human Otc Drug

Ibuprofen
NDC 11822-0291

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

Pain Relief Ibuprofen
NDC 11822-0292

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

Pain Relief Ibuprofen
NDC 11822-0392

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

Ibuprofen
NDC 11822-0393

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

Pain Relief Aspirin Low Dose
NDC 11822-0600

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

Laxative For Women
NDC 11822-0676

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

Laxative
NDC 11822-0790

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

All Day Allergy
NDC 11822-1002

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

Rugby Laboratories

NDC Product
Human Otc Drug

Aspirin Regular Strength
NDC 0536-1232

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

Aspirin Low Dose
NDC 0536-1234

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

Acetaminophen, Aspirin, Caffeine
NDC 0536-1326

Generic Name
Acetaminophen, Aspirin, Caffeine
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

SpecGx LLC

NDC Product
Human Prescription Drug

Morphine Sulfate
NDC 0406-8315

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

Morphine Sulfate
NDC 0406-8320

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

Morphine Sulfate
NDC 0406-8330

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

Morphine Sulfate
NDC 0406-8380

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

Morphine Sulfate
NDC 0406-8390

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

TARGET CORPORATION

NDC Product
Human Otc Drug

Dual Action Pain Relief
NDC 11673-924

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

Target Corporation

NDC Product
Human Otc Drug

Menstrual Relief
NDC 11673-390

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

Up And Up Allergy Relief
NDC 11673-502

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

Teva Pharmaceuticals USA, Inc.

NDC Product
Human Prescription Drug

Amoxicillin And Clavulanate Potassium
NDC 0093-2274

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

Amoxicillin And Clavulanate Potassium
NDC 0093-2275

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

Amoxicillin And Clavulanate Potassium
NDC 0093-2277

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

Amoxicillin And Clavulanate Potassium
NDC 0093-2279

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

Hydroxyzine Hydrochloride
NDC 0093-5060

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

Hydroxyzine Hydrochloride
NDC 0093-5061

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

Hydroxyzine Hydrochloride
NDC 0093-5062

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

Almotriptan Malate
NDC 0093-5260

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

Almotriptan Malate
NDC 0093-5261

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

Raloxifene Hydrochloride
NDC 0093-7290

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

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

Famciclovir
NDC 0093-8117

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

NDC 0093-8117

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

Famciclovir
NDC 0093-8118

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

NDC 0093-8118

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

Famciclovir
NDC 0093-8119

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

NDC 0093-8119

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

Quetiapine
NDC 0093-8162

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

Quetiapine
NDC 0093-8163

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

Quetiapine
NDC 0093-8164

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

Quetiapine
NDC 0093-8165

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

Quetiapine
NDC 0093-8166

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

Eletriptan Hydrobromide
NDC 0093-8310

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

Eletriptan Hydrobromide
NDC 0093-8311

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

Kariva
NDC 0555-9050

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

WALGREEN COMPANY

NDC Product
Human Otc Drug

Acetaminophen And Ibuprofen
NDC 0363-4081

Generic Name
Acetaminophen And Ibuprofen
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
ANDA
Active Listing

WALGREENS

NDC Product
Human Otc Drug

Acetaminophen And Ibuprofen
NDC 0363-9131

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

Walgreen Company

NDC Product
Human Otc Drug

Ibuprofen
NDC 0363-0291

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

Ibuprofen
NDC 0363-0292

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

Dye Free Ibuprofen
NDC 0363-0438

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

Aspirin Enteric Coated Low Dose
NDC 0363-0563

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

Aspirin
NDC 0363-0587

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

Aspirin 325
NDC 0363-0691

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

Nasal Decongestant D
NDC 0363-1214

Generic Name
Pseudoephedrine Hcl
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Menstrual Pain Relief
NDC 0363-3900

Generic Name
Acetaminophen, Caffeine, Pyrilamine Maleate
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Menstrual Relief
NDC 0363-3909

Generic Name
Acetaminophen, Caffeine, Pyrilamine Maleate
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Allergy Relief
NDC 0363-4101

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

Dye Free Ibuprofen
NDC 0363-4381

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

Sinus Pe Congestion
NDC 0363-4534

Generic Name
Diphenhydramine Hcl, Phenylephrine Hcl
Dosage Form
Kit
Route
N/A
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Allergy Relief Plus Congestion
NDC 0363-4851

Generic Name
Diphenhydramine Hcl, Phenylephrine Hcl
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Allergy Relief
NDC 0363-5430

Generic Name
Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Ephedrine Sulfate
NDC 0363-5789

Generic Name
Ephedrine Sulfate
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Aspirin Enteric Coated Low Dose
NDC 0363-6450

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

Laxative
NDC 0363-6760

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

Menstrual Complete Pain Relief
NDC 0363-9390

Generic Name
Acetaminophen, Caffeine, Pyrilamine Maleate
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
OTC MONOGRAPH DRUG
Active Listing

Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.

NDC Product
Human Prescription Drug

Duavee
NDC 0008-1123

Generic Name
Conjugated Estrogens/bazedoxifene
Dosage Form
Tablet, Film Coated
Route
Oral
Marketing
NDA
Active Listing

External Clinical & Regulatory Resources

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