NDC 0143-9787 – Enalaprilat

Enalaprilat Dihydrate 1.25 mg/mL · Injection · Intravenous

Human Prescription Drug

Product NDC0143-9787

Product details

Brand name
Enalaprilat
Generic name
Enalaprilat
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Injection
Route
Intravenous
Marketing category
ANDA · ANDA078687
Marketed since
December 23, 2008
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Enalaprilat →

Package NDC codes (1)

Package NDCDescriptionSince
0143-9787-1010 VIAL in 1 CARTON (0143-9787-10) / 1 mL in 1 VIAL (0143-9787-01)Dec 23, 2008

Other Enalaprilat products