Valsartan and Hydrochlorothiazide

Basic Information

Product Name

FDA Product Code

53746-849

Regulatory Information

NDC Product Code

53746-849

Application Number

ANDA204382

Marketing Category

C73584

Effective Date

May 8, 2023

Territorial Authority

USA

FDA Title

These highlights do not include all the information needed to use VALSARTAN AND HYDROCHLOROTHIAZIDE TABLETS safely and effectively. See full prescribing information for . for oral use Initial U.S. Approval:1998

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Version Number

Active Ingredients

HYDROCHLOROTHIAZIDE

Quantity: 25 mg in 1 1

Code: 0J48LPH2TH

Class Code: ACTIB

CROSCARMELLOSE SODIUM

Code: M28OL1HH48

Class Code: IACT

FERRIC OXIDE YELLOW

Code: EX438O2MRT

Class Code: IACT

HYPROMELLOSES

Code: 3NXW29V3WO

Class Code: IACT

VALSARTAN

Quantity: 320 mg in 1 1

Code: 80M03YXJ7I

Class Code: ACTIB

CELLULOSE, MICROCRYSTALLINE

Code: OP1R32D61U

Class Code: IACT

MAGNESIUM STEARATE

Code: 70097M6I30

Class Code: IACT

POLYVINYL ALCOHOL, UNSPECIFIED

Code: 532B59J990

Class Code: IACT

POLYETHYLENE GLYCOL, UNSPECIFIED

Code: 3WJQ0SDW1A

Class Code: IACT

SILICON DIOXIDE

Code: ETJ7Z6XBU4

Class Code: IACT

TALC

Code: 7SEV7J4R1U

Class Code: IACT

TITANIUM DIOXIDE

Code: 15FIX9V2JP

Class Code: IACT

Active Moieties

VALSARTAN

Code: 80M03YXJ7I

HYDROCHLOROTHIAZIDE

Code: 0J48LPH2TH

Basic Information

Regulatory Information

Company Information

Active Ingredients

CROSCARMELLOSE SODIUM

FERRIC OXIDE YELLOW

HYPROMELLOSES

CELLULOSE, MICROCRYSTALLINE

MAGNESIUM STEARATE

POLYVINYL ALCOHOL, UNSPECIFIED

POLYETHYLENE GLYCOL, UNSPECIFIED

SILICON DIOXIDE

TALC

TITANIUM DIOXIDE

Active Moieties

VALSARTAN

HYDROCHLOROTHIAZIDE