FDA NDC Directory · JSON-LD · Markdown

Paclitaxel

NDC 68001-705 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA216874
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsPACLITAXEL (6 mg/mL)
Marketing started20260401
Package count1

External sources

Source: openFDA. Public-domain (CC0).