FDA NDC Directory · JSON-LD · Markdown

AZITHROMYCIN DIHYDRATE

NDC 72189-090 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDIRECT RX
Marketing categoryAbbreviated NDA (generic) · App ANDA208249
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAZITHROMYCIN DIHYDRATE (500 mg/1)
Marketing started20200522
Marketing ended20261031
Package count2

External sources

Source: openFDA. Public-domain (CC0).