United States · FDA National Drug Code directory
Ramipril
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0054-0109_8a7f6a6e-70a7-43ce-9f85-e60e237246ba
- Product NDC
- 0054-0109
- Form
- CAPSULE
- Composition / generic term
- Ramipril
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20080618
- Source listing expiry
- 20271231
Source-listed ingredients
- RAMIPRIL — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (0054-0109-25) · 0054-0109-25
- 500 CAPSULE in 1 BOTTLE (0054-0109-29) · 0054-0109-29
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →