FDA NDC Directory · JSON-LD · Markdown

AZITHROMYCIN

NDC 68788-7549 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerPreferred Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207531
Dosage form / routePOWDER, FOR SUSPENSION · PARENTERAL
Active ingredientsAZITHROMYCIN MONOHYDRATE (200 mg/5mL)
Marketing started20180410
Package count1

External sources

Source: openFDA. Public-domain (CC0).