FDA NDC Directory · JSON-LD · Markdown
NDC 68001-651 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION
| Generic name | Paclitaxel |
|---|---|
| Labeler / Manufacturer | BluePoint Laboratories |
| Marketing category | Abbreviated NDA (generic) · App ANDA216355 |
| Dosage form / route | INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION · INTRAVENOUS |
| Active ingredients | PACLITAXEL (100 mg/20mL) |
| Marketing started | 20250718 |
| Package count | 1 |
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