NDC 55566-1010
Fyremadel 250 ug per 0.5 mL injection, solution
On the label: Ferring Pharmaceuticals 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 Ferring Pharmaceuticals Inc. names for other drugs.
Recalls
- Apr 19, 2023 · Class II · Sun Pharmaceutical Industries Ltd.
Presence of Particulate Matter: A piece of glass was found in a prefilled syringe.
Lots: Lot #: HAD1190A, Exp. 02/2024
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ganirelix: every company that makes it
- Form
- injection, solution, subcutaneous
- Strength
- 250 ug per 0.5 mL
- Approval
- ANDA ANDA204246
- On the market since
- Feb 28, 2022
- Package NDCs
55566-1010-1- Official label
- DailyMed (National Library of Medicine), updated Oct 16, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?