NDC 0409-6531 – Vancomycin Hydrochloride

Vancomycin Hydrochloride 750 mg/1 · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug 5 recalls

Product NDC0409-6531

Product details

Brand name
Vancomycin Hydrochloride
Generic name
Vancomycin Hydrochloride
Labeler
Hospira, Inc.
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
ANDA · ANDA062912
Marketed since
March 27, 2009
Listing expires
December 31, 2027
Pharmacologic class
Glycopeptide Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Vancomycin Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
0409-6531-0210 VIAL in 1 TRAY (0409-6531-02) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0409-6531-12)Mar 27, 2009

Recalls mentioning this NDC

Other Vancomycin Hydrochloride products