Skip to main content

Enalapril Maleate

NDC 51672-4245 · Sun Pharmaceutical Industries, Inc.

Generic nameEnalapril Maleate
Dosage formTABLET
RouteORAL
Active ingredient(s)ENALAPRIL MALEATE
Strength10 mg/1
Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]
Marketing categoryANDA

Packages

51672-4245-1 — 100 TABLET in 1 BOTTLE (51672-4245-1)

51672-4245-3 — 1000 TABLET in 1 BOTTLE (51672-4245-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51407-828 — Enalapril Maleate, 51655-006 — Enalapril maleate, 51655-058 — Enalapril maleate, 51655-110 — Enalapril maleate, 51655-341 — Enalapril Maleate, 51672-4037 — Enalapril Maleate, 51672-4038 — Enalapril Maleate, 51672-4040 — Enalapril Maleate, 51672-4045 — Enalapril Maleate and Hydrochlorothiazide, 51672-4046 — Enalapril Maleate and Hydrochlorothiazide, 52536-401 — Enalapril maleate, 52652-4001 — enalapril maleate, 55111-133 — Enalapril maleate and hydrochlorothiazide, 55111-134 — Enalapril maleate and hydrochlorothiazide, 59651-529 — ENALAPRIL MALEATE, 60429-183 — Enalapril Maleate, 60429-184 — Enalapril Maleate, 60429-186 — Enalapril Maleate, 60760-575 — Enalapril Maleate, 62135-589 — Enalapril maleate, +89 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.