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LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE

Losartan Potassium and Hydrochlorothiazide Tablets, USP

Approved
Approval ID

27badbda-3635-444e-8005-5d5ee16f8c3c

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Apr 13, 2011

Manufacturers
FDA

Rebel Distributors Corp

DUNS: 118802834

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code21695-831
Application NumberANDA078385
Product Classification
M
Marketing Category
C73584
G
Generic Name
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
Product Specifications
Route of AdministrationORAL
Effective DateOctober 26, 2010
FDA Product Classification

INGREDIENTS (13)

LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
HYDROCHLOROTHIAZIDEActive
Quantity: 25 mg in 1 1
Code: 0J48LPH2TH
Classification: ACTIB
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTEDInactive
Code: 2165RE0K14
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
LOSARTAN POTASSIUMActive
Quantity: 100 mg in 1 1
Code: 3ST302B24A
Classification: ACTIB
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
POLYETHYLENE GLYCOLInactive
Code: 3WJQ0SDW1A
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT

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LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE - FDA Drug Approval Details