FDA NDC Directory · JSON-LD · Markdown

Bortezomib

NDC 68083-650 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerGland Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA219167
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS SUBCUTANEOUS
Active ingredientsBORTEZOMIB (1 mg/1)
Marketing started20260106
Package count1

External sources

Source: openFDA. Public-domain (CC0).