Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Meridian Medical Technologies, LLC | St. Louis, MO, United States | Makes it, tests it, packages it, labels it and sterilizes it | Problems found, fixed voluntarilyJun 30, 2026 · 21 inspections, 9 with FDA action |
Recalls
- Jun 6, 2012 · Class II · Meridian Medical Technologies a Pfizer Company
Impurities/Degradation Products: High Out of Specification levels for carbostyril, a known degradation product of diazepam.
Lots: Lot #: 8D1082, Exp 01/13; 8D1151, Exp 03/13
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, intramuscular
- Strength
- 10 mg per 2 mL
- Approval
- NDA NDA020124
- On the market since
- Dec 5, 1990
- Package NDCs
11704-600-01- Official label
- DailyMed (National Library of Medicine), updated Dec 18, 2023
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