Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| West-Ward Columbus Inc. | Columbus, OH, United States | Makes it | No problems foundApr 30, 2026 · 27 inspections |
Recalls
- Aug 24, 2026 · Class II · Hikma Pharmaceuticals USA INC.
Failed Impurities/Degradation Specifications: OOS result obtained for a process impurity, dicyclohexylurea (DCU).
Lots: a) Lot #: AC5470A, Exp. Date July 2027 b) Lot #: AC5470B, Exp. Date July 2027
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ramiprilat: every company that makes it
- Form
- capsule, oral
- Strength
- 2.5 mg
- Approval
- ANDA ANDA077900
- On the market since
- Jun 18, 2008
- Package NDCs
76282-671-0176282-671-05- Official label
- DailyMed (National Library of Medicine), updated Oct 1, 2021
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