FDA NDC Directory · JSON-LD · Markdown

Azithromycin Dihydrate

NDC 72789-081 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208250
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAZITHROMYCIN DIHYDRATE (250 mg/1)
Marketing started20190701
Marketing ended20261130
Package count1

External sources

Source: openFDA. Public-domain (CC0).