NDC 0409-6533

Vancomycin Hydrochloride 1 g injection, powder, lyophilized, for solution

On the label: Hospira, Inc..

Where it's made

McPherson, KS, United States · makes it, tests it, packages it and labels it

Problems found, fixed voluntarily Last FDA inspection Jan 17, 2025. 16 inspections on record, 2 with serious problems.

Dec 22, 2022 · Class I · Terminated
Presence of Particulate Matter: Glass particulate matter detected in injectable.
Lots: Lot: 33045BA, EXP 1SEP2023
Aug 30, 2017 · Class I · Terminated
Presence of Particulate Matter: glass particulate found in vial
Lots: Lot: 632153A; Exp. 03/18
Nov 7, 2014 · Class III · Terminated
Correct Labeled Product Mispack: Product tray containing vials was mislabeled to contain another product.
Lots: Lot# 43-240-DD; Exp. 07/16 Lot# 44-205-DD,44-455-DD,44-460-DD,44-465-DD; Exp. 08/16
Oct 6, 2014 · Class II · Terminated
Temperature Abuse: Products experienced uncontrolled temperature excursions during transit.
Lots: One shipment of Lot #: 34-366-8E02; Exp 1OCT2015 to The Harvard Drug Group, Livonia, MI
Oct 6, 2014 · Class II · Terminated
Temperature Abuse: Products experienced uncontrolled temperature excursions during transit.
Lots: Lot #: 35-315-DD; Exp 1NOV2015

Generic drug: Vancomycin: see every company that makes it
Form: injection, powder, lyophilized, for solution, intravenous
Strength: 1 g
Approval: ANDA ANDA062912
On the market since: Feb 18, 2020
Package NDCs: 0409-6533-31 0409-6533-59
Official label: DailyMed (National Library of Medicine), updated Apr 1, 2026

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