FDA NDC Directory · JSON-LD · Markdown
NDC 55111-686 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
| Labeler / Manufacturer | Dr. Reddy's Laboratories Limited |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA091365 |
| Dosage form / route | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS |
| Active ingredients | GEMCITABINE HYDROCHLORIDE (200 mg/5mL) |
| Marketing started | 20110725 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).