FDA NDC Directory · JSON-LD · Markdown
NDC 70095-025 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
| Labeler / Manufacturer | Sun Pharmaceutical Industries Limited |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA065501 |
| Dosage form / route | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS |
| Active ingredients | AZITHROMYCIN MONOHYDRATE (500 mg/10mL) |
| Marketing started | 20230327 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).