FDA NDC Directory · JSON-LD · Markdown

Losortan Potassium

NDC 50268-504 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameLosartan Potassium
Labeler / ManufacturerAvPAK
Marketing categoryAbbreviated NDA (generic) · App ANDA078243
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLOSARTAN POTASSIUM (25 mg/1)
Marketing started20200529
Package count1

External sources

Source: openFDA. Public-domain (CC0).