NDC 69097-856 – Fosinopril Sodium

Fosinopril Sodium 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC69097-856

Product details

Brand name
Fosinopril Sodium
Generic name
Fosinopril
Labeler
Cipla USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077222
Marketed since
June 16, 2016
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
69097-856-0590 TABLET in 1 BOTTLE (69097-856-05)Jun 16, 2016
69097-856-151000 TABLET in 1 BOTTLE (69097-856-15)Jun 16, 2016

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