Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | McPherson, KS, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJan 17, 2025 · 16 inspections, 2 with FDA action |
Recalls
- Jun 23, 2016 · Class II · Hospira Inc.
Crystallization: Product contains particulate identified to be crystallized active ingredient.
Lots: Lot #: 52610LL, Exp. 01 OCT 2016; Lot #: 57660LL, Exp. 01 MAR 2017
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Diazepam: every company that makes it
- Form
- injection, solution, intramuscular; intravenous
- Strength
- 5 mg per 1 mL
- Approval
- ANDA ANDA072079
- On the market since
- Aug 23, 2005
- Package NDCs
0409-1273-030409-1273-32- Official label
- DailyMed (National Library of Medicine), updated Jan 5, 2024
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