Class II · Moderate risk
Dihydroergotamine Mesylate Injection
Discoloration
National Drug Code
Is NDC 81284-0411-05 recalled?
Dihydroergotamine Mesylate · 5 AMPULE in 1 CARTON (81284-411-05) / 1 mL in 1 AMPULE (81284-411-00)
Yes — this exact package was recalled
1 FDA recall names the code 81284-0411-05 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.
1 of these recalls is still ongoing.
- Active ingredient
- Dihydroergotamine Mesylate
- Strength
- DIHYDROERGOTAMINE MESYLATE 1 mg/mL
- Form
- Injection, Solution · Intramuscular, Intravenous, Subcutaneous
- Labeler
- Provepharm Inc.
- Type
- Human Prescription Drug
- Product code
- 81284-0411
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.
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