United States · FDA National Drug Code directory

Enalaprilat

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
0143-9786_bde8c35d-1cf2-42ea-a2a7-c4eb165e6d0d
Product NDC
0143-9786
Form
INJECTION
Composition / generic term
enalaprilat
Labeler
Hikma Pharmaceuticals USA Inc.
Marketing category
ANDA
Marketing start / end (source format)
20081223
Source listing expiry
20261231

Source-listed ingredients

  • ENALAPRILAT DIHYDRATE — 2.5 mg/2mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 VIAL in 1 CARTON (0143-9786-10) / 2 mL in 1 VIAL (0143-9786-01) · 0143-9786-10

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 →