Class II ยท Moderate risk
Revonto (dantrolene sodium for injection)
cGMP deviations: Temperature abuse
National Drug Code
Is NDC 78670-0003-67 recalled?
Revonto · 6 VIAL, GLASS in 1 CARTON (78670-003-67) / 60 mL in 1 VIAL, GLASS
Yes — this exact package was recalled
1 FDA recall names the code 78670-0003-67 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
- dantrolene sodium
- Strength
- DANTROLENE SODIUM 20 mg/60mL
- Form
- Injection, Powder, Lyophilized, for Solution · Intravenous
- Labeler
- Uswm, LLC
- Type
- Human Prescription Drug
- Product code
- 78670-0003
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
- 78670-0130 See recall 1
- 78670-0131 See recall 1
Free recall alerts
Know the day your medication is recalled
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