FDA NDC Directory · JSON-LD · Markdown

azithromycin

NDC 0904-7351 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA065399
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAZITHROMYCIN DIHYDRATE (500 mg/1)
Marketing started20230501
Package count1

External sources

Source: openFDA. Public-domain (CC0).