NDC 71335-9703 – Fosinopril sodium

Fosinopril Sodium 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-9703

Product details

Brand name
Fosinopril sodium
Generic name
Fosinopril sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205670
Marketed since
October 1, 2017
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 (3)

Package NDCDescriptionSince
71335-9703-130 TABLET in 1 BOTTLE (71335-9703-1)May 11, 2023
71335-9703-290 TABLET in 1 BOTTLE (71335-9703-2)May 11, 2023
71335-9703-328 TABLET in 1 BOTTLE (71335-9703-3)May 11, 2023

Other Fosinopril Sodium products