NDC 63323-821 – Bortezomib

Bortezomib 3.5 mg/1 · Injection, Powder, Lyophilized, For Solution · Intravenous, Subcutaneous

Human Prescription Drug

Product NDC63323-821

Product details

Brand name
Bortezomib
Generic name
Bortezomib
Labeler
Fresenius Kabi USA, LLC
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous, Subcutaneous
Marketing category
ANDA · ANDA209659
Marketed since
May 2, 2022
Listing expires
December 31, 2026
Pharmacologic class
Proteasome Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Bortezomib →

Package NDC codes (1)

Package NDCDescriptionSince
63323-821-101 VIAL, SINGLE-USE in 1 CARTON (63323-821-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USEMay 2, 2022

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