NDC 51672-4040 – Enalapril Maleate

Enalapril Maleate 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51672-4040

Product details

Brand name
Enalapril Maleate
Generic name
Enalapril Maleate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075657
Marketed since
January 23, 2001
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
51672-4040-1100 TABLET in 1 BOTTLE (51672-4040-1)Jan 23, 2001
51672-4040-31000 TABLET in 1 BOTTLE (51672-4040-3)Jan 23, 2001

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