United States · FDA National Drug Code directory

Enalapril Maleate

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
71205-075_bdfcb7c8-7269-46a6-aff8-d73b093ee88a
Product NDC
71205-075
Form
TABLET
Composition / generic term
Enalapril Maleate
Labeler
Proficient Rx LP
Marketing category
NDA AUTHORIZED GENERIC
Marketing start / end (source format)
19851224
Source listing expiry
20261231

Source-listed ingredients

  • ENALAPRIL MALEATE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (71205-075-30) · 71205-075-30
  • 60 TABLET in 1 BOTTLE (71205-075-60) · 71205-075-60
  • 90 TABLET in 1 BOTTLE (71205-075-90) · 71205-075-90

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 →