Class I ยท High risk
Midazolam Injection
Labeling: Label MIX-UP. Blister Packages, Labeled as Midazolam injection, USP, 2 mg / 2 ml, Containing Syringes of Ondansetron Injection, USP, 4 mg / 2 mL
National Drug Code
Is NDC 76045-0001-20 recalled?
Midazolam · 24 BLISTER PACK in 1 CARTON (76045-001-20) / 1 SYRINGE, GLASS in 1 BLISTER PACK (76045-001-00) / 2 mL in 1 SYRINGE, GLASS
Yes — this exact package was recalled
1 FDA recall names the code 76045-0001-20 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
- Midazolam Hydrochloride
- Strength
- MIDAZOLAM HYDROCHLORIDE 2 mg/2mL
- Form
- Injection, Solution · Intramuscular, Intravenous
- Labeler
- Fresenius Kabi USA, LLC
- Type
- Human Prescription Drug · DEA CIV
- Product code
- 76045-0001
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.
Other recalled products from this labeler
- 76045-0004 Morphine Sulfate 1
Free recall alerts
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