FDA NDC Directory · JSON-LD · Markdown

Losartan Potassium

NDC 68084-347 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA078243
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLOSARTAN POTASSIUM (50 mg/1)
Marketing started20101012
Package count1

External sources

Source: openFDA. Public-domain (CC0).