NDC 59651-104
Eletriptan Hydrobromide 20 mg tablet, film coated
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Tirupati, India | Makes it and tests it | Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections |
Recalls
- Mar 15, 2021 · Class II · Cardinal Health Inc.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots: EA2020001-A
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Eletriptan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA210708
- On the market since
- Jan 15, 2019
- Package NDCs
59651-104-0659651-104-69- Official label
- DailyMed (National Library of Medicine), updated Jun 3, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?