United States · FDA National Drug Code directory
Moexipril Hydrochloride
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
- 62135-967_3001c14d-1545-86fb-e063-6294a90a035f
- Product NDC
- 62135-967
- Form
- TABLET, FILM COATED
- Composition / generic term
- Moexipril Hydrochloride
- Labeler
- Chartwell RX, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20061130
- Source listing expiry
- 20261231
Source-listed ingredients
- MOEXIPRIL HYDROCHLORIDE — 7.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET, FILM COATED in 1 BOTTLE (62135-967-90) · 62135-967-90
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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