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
63187-816_cd41f0ae-d2bb-4ffc-9a5e-7ca6345cbe89
Product NDC
63187-816
Form
CAPSULE
Composition / generic term
Ramipril
Labeler
Proficient Rx LP
Marketing category
ANDA
Marketing start / end (source format)
20110608
Source listing expiry
20261231

Source-listed ingredients

  • RAMIPRIL — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 CAPSULE in 1 BOTTLE (63187-816-30) · 63187-816-30
  • 60 CAPSULE in 1 BOTTLE (63187-816-60) · 63187-816-60
  • 90 CAPSULE in 1 BOTTLE (63187-816-90) · 63187-816-90

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 →