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ENALAPRIL MALEATE

NDC 50228-230 · ScieGen Pharmaceuticals, 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

50228-230-01 — 100 TABLET in 1 BOTTLE (50228-230-01)

50228-230-10 — 1000 TABLET in 1 BOTTLE (50228-230-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-4560 — Enalapril Maleate, 50090-6437 — Enalapril maleate, 50090-6490 — enalapril maleate, 50090-6712 — Enalapril Maleate, 50090-7222 — Enalapril maleate, 50090-7302 — Enalapril Maleate, 50090-7677 — ENALAPRIL MALEATE, 50090-7678 — ENALAPRIL MALEATE, 50228-228 — ENALAPRIL MALEATE, 50228-229 — ENALAPRIL MALEATE, 50228-231 — ENALAPRIL MALEATE, 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, +89 more

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