NDC 76282-200 – Fosinopril sodium

Fosinopril Sodium 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC76282-200

Product details

Brand name
Fosinopril sodium
Generic name
Fosinopril sodium
Labeler
Exelan Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077222
Marketed since
June 21, 2005
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fosinopril Sodium →

Package NDC codes (2)

Package NDCDescriptionSince
76282-200-101000 TABLET in 1 BOTTLE (76282-200-10)Jun 21, 2005
76282-200-9090 TABLET in 1 BOTTLE (76282-200-90)Jun 21, 2005

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