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Azithromycin

NDC 0781-8091 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerSandoz Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA065209
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAZITHROMYCIN DIHYDRATE (600 mg/1)
Marketing started20051114
Package count1

External sources

Source: openFDA. Public-domain (CC0).