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
76282-673_37481fc5-771f-4dc7-aa06-6913ab75d485
Product NDC
76282-673
Form
CAPSULE
Composition / generic term
Ramipril
Labeler
Exelan Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20080618
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 (76282-673-01) · 76282-673-01
  • 500 CAPSULE in 1 BOTTLE (76282-673-05) · 76282-673-05

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.

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