FDA NDC Directory · JSON-LD · Markdown

AZITHROMYCIN

NDC 24658-708 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerPURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS
Marketing categoryAbbreviated NDA (generic) · App ANDA207531
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsAZITHROMYCIN MONOHYDRATE (200 mg/5mL)
Marketing started20200430
Package count1

External sources

Source: openFDA. Public-domain (CC0).