NDC 71335-0381 – Fosinopril Sodium

Fosinopril Sodium 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0381

Product details

Brand name
Fosinopril Sodium
Generic name
Fosinopril
Labeler
Bryant Ranch Prepack
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 (4)

Package NDCDescriptionSince
71335-0381-130 TABLET in 1 BOTTLE (71335-0381-1)Feb 9, 2022
71335-0381-290 TABLET in 1 BOTTLE (71335-0381-2)Feb 9, 2022
71335-0381-360 TABLET in 1 BOTTLE (71335-0381-3)Feb 9, 2022
71335-0381-428 TABLET in 1 BOTTLE (71335-0381-4)Feb 9, 2022

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