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Azithromycin

NDC 68071-5082 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207398
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAZITHROMYCIN DIHYDRATE (500 mg/1)
Marketing started20180705
Package count2

External sources

Source: openFDA. Public-domain (CC0).