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azithromycin dihydrate

NDC 80425-0431 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA065398
Dosage form / routeTABLET · ORAL
Active ingredientsAZITHROMYCIN DIHYDRATE (250 mg/1)
Marketing started20240827
Package count1

External sources

Source: openFDA. Public-domain (CC0).