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Paclitaxel

NDC 46708-621 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA216874
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsPACLITAXEL (6 mg/mL)
Marketing started20221020
Package count1

External sources

Source: openFDA. Public-domain (CC0).