NDC 68682-712 – Enalapril Maleate

Enalapril Maleate 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68682-712

Product details

Brand name
Enalapril Maleate
Generic name
Enalapril Maleate
Labeler
OCEANSIDE PHARMACEUTICALS
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA018998
Marketed since
December 24, 1985
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Enalapril maleate →

Package NDC codes (2)

Package NDCDescriptionSince
68682-712-01100 TABLET in 1 BOTTLE (68682-712-01)Dec 24, 1985
68682-712-101000 TABLET in 1 BOTTLE (68682-712-10)Dec 24, 1985

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