"62332-049-30" National Drug Code (NDC)

Losartan Potassium And Hydrochlorothiazide 30 TABLET, FILM COATED in 1 BOTTLE (62332-049-30)
(Alembic Pharmaceuticals Inc.)

NDC Code62332-049-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (62332-049-30)
Product NDC62332-049
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLosartan Potassium And Hydrochlorothiazide
Non-Proprietary NameLosartan Potassium And Hydrochlorothiazide
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20160523
Marketing Category NameANDA
Application NumberANDA091617
ManufacturerAlembic Pharmaceuticals Inc.
Substance NameHYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
Strength12.5; 100
Strength Unitmg/1; mg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]

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