FDA NDC Directory · JSON-LD · Markdown

azithromycin

NDC 70518-4356 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA065398
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAZITHROMYCIN DIHYDRATE (250 mg/1)
Marketing started20250613
Package count1

External sources

Source: openFDA. Public-domain (CC0).