NDC 61703-323 – Bleomycin

Bleomycin Sulfate 30 [USP'U]/1 · Injection, Powder, Lyophilized, For Solution · Intramuscular, Intrapleural, Intravenous, Subcutaneous

Human Prescription Drug 1 recall

Product NDC61703-323

Product details

Brand name
Bleomycin
Generic name
Bleomycin
Labeler
Hospira, Inc.
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intramuscular, Intrapleural, Intravenous, Subcutaneous
Marketing category
ANDA · ANDA065031
Marketed since
April 10, 2000
Listing expires
December 31, 2026
Pharmacologic class
Cytoprotective Agent

Active ingredients

Uses, dosage, side effects and warnings for Bleomycin →

Package NDC codes (1)

Package NDCDescriptionSince
61703-323-221 VIAL, SINGLE-DOSE in 1 CARTON (61703-323-22) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSEApr 10, 2000

Recalls mentioning this NDC

Other Bleomycin products