Class II ยท Moderate risk
Rocuronium Bromide Injection 50mg/5 mL
Labeling: Label Lacks Warning or Rx Legend: Finished product did not include the statement on the flip cap vial, "WARNING: PARALYZING AGENT"
National Drug Code
Is NDC 66794-0228-41 recalled?
Rocuronium · 10 VIAL in 1 CARTON (66794-228-41) / 5 mL in 1 VIAL (66794-228-02)
Yes — this exact package was recalled
1 FDA recall names the code 66794-0228-41 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
- Rocuronium
- Strength
- ROCURONIUM BROMIDE 50 mg/5mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Piramal Critical Care Inc
- Type
- Human Prescription Drug
- Product code
- 66794-0228
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
- 66794-0015 Sevoflurane 1
- 66794-0151 Gablofen 1
- 66794-0206 See recall 1
- 66794-0207 See recall 1
- 66794-0208 See recall 1
- 66794-0209 See recall 1
Free recall alerts
Know the day your medication is recalled
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