Class II ยท Moderate risk
Diazepam Injection
Impurities/Degradation Products: High Out of Specification levels for carbostyril, a known degradation product of diazepam.
National Drug Code
Is NDC 11704-0600-01 recalled?
Diazepam · 1 SYRINGE, GLASS in 1 POUCH (11704-600-01) / 2 mL in 1 SYRINGE, GLASS
Yes — this exact package was recalled
1 FDA recall names the code 11704-0600-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- diazepam
- Strength
- DIAZEPAM 10 mg/2mL
- Form
- Injection · Intramuscular
- Labeler
- Meridian Medical Technologies LLC
- Type
- Human Prescription Drug · DEA CIV
- Product code
- 11704-0600
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Free recall alerts
Know the day your medication is recalled
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