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Azithromycin

NDC 55695-003 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerSTATE HEALTH SERVICES, TEXAS DEPARTMENT OF
Marketing categoryAbbreviated NDA (generic) · App ANDA065246
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsAZITHROMYCIN MONOHYDRATE (200 mg/5mL)
Marketing started20101217
Package count2

External sources

Source: openFDA. Public-domain (CC0).