NDC 81284-411
Dihydroergotamine Mesylate 1 mg per 1 mL injection, solution
On the label: Provepharm Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Provepharm Inc. names for other drugs.
Recalls
- Nov 22, 2024 · Class II · Provepharm Inc.
Discoloration
Lots: Lot #: F9026F01, F9026F02, Exp. Date 12/2025
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Dihydroergotamine: every company that makes it
- Form
- injection, solution, intramuscular; intravenous; subcutaneous
- Strength
- 1 mg per 1 mL
- Approval
- ANDA ANDA212046
- On the market since
- Sep 30, 2021
- Package NDCs
81284-411-0081284-411-0581284-411-10- Official label
- DailyMed (National Library of Medicine), updated Feb 25, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?