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Azithromycin

NDC 50111-789 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065218
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAZITHROMYCIN MONOHYDRATE (600 mg/1)
Marketing started20051201
Package count1

External sources

Source: openFDA. Public-domain (CC0).