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
51407-709_9f641c30-6ffa-4765-8991-cc15976b111d
Product NDC
51407-709
Form
CAPSULE
Composition / generic term
Ramipril
Labeler
GSMS, Incorporated
Marketing category
ANDA
Marketing start / end (source format)
20250708
Source listing expiry
20261231

Source-listed ingredients

  • RAMIPRIL — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 CAPSULE in 1 BOTTLE (51407-709-01) · 51407-709-01

Source and coverage

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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.

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