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Enalapril maleate

NDC 51655-110 · Northwind Health Company, LLC

Generic nameEnalapril maleate
Dosage formTABLET
RouteORAL
Active ingredient(s)ENALAPRIL MALEATE
Strength5 mg/1
Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]
Marketing categoryANDA

Packages

51655-110-26 — 90 TABLET in 1 BOTTLE, PLASTIC (51655-110-26)

51655-110-52 — 30 TABLET in 1 BOTTLE, PLASTIC (51655-110-52)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-7302 — Enalapril Maleate, 50090-7677 — ENALAPRIL MALEATE, 50090-7678 — ENALAPRIL MALEATE, 50228-228 — ENALAPRIL MALEATE, 50228-229 — ENALAPRIL MALEATE, 50228-230 — ENALAPRIL MALEATE, 50228-231 — ENALAPRIL MALEATE, 51407-828 — Enalapril Maleate, 51655-006 — Enalapril maleate, 51655-058 — 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, 51672-4245 — Enalapril Maleate, 52536-401 — Enalapril maleate, 52652-4001 — enalapril maleate, 55111-133 — Enalapril maleate and hydrochlorothiazide, +89 more

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