ALFUZOSIN HYDROCHLORIDE

Manufacturing Establishments (1)

Labeler

DirectRX

DUNS Number

079254320

NDC Product Code

61919-349

Application Number

ANDA079057

Marketing Category

ANDA (C73584)

Route of Administration

ORAL

Effective Date

January 17, 2020

Ingredients

STARCH, CORNInactive

Code: O8232NY3SJClass: IACT

HYPROMELLOSESInactive

Code: 3NXW29V3WOClass: IACT

SILICON DIOXIDEInactive

Code: ETJ7Z6XBU4Class: IACT

DIMETHYLAMINOETHYL METHACRYLATE - BUTYL METHACRYLATE - METHYL METHACRYLATE COPOLYMERInactive

Code: 905HNO1SIHClass: IACT

MAGNESIUM STEARATEInactive

Code: 70097M6I30Class: IACT

Code: 75046A1XTNClass: ACTIBQuantity: 10 mg in 1 1

HYDROXYPROPYL CELLULOSE (1600000 WAMW)Inactive

Code: RFW2ET671PClass: IACT

TALCInactive

Code: 7SEV7J4R1UClass: IACT