Hospira, Inc.
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.
NDC 0409-5017
Vancomycin Hydrochloride 500 mg per 5 mL injection, powder, lyophilized, for solution
On the label: Hospira, Inc..
Where it's made
Product details
- Generic drug
- Vancomycin: see every company that makes it
- Form
- injection, powder, lyophilized, for solution
- Strength
- 500 mg per 5 mL
- Approval
- ANDA ANDA063076
- On the market since
- Nov 2, 2021
- Package NDCs
0409-5017-01- Official label
- DailyMed (National Library of Medicine), updated Jul 20, 2026
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