NDC 71335-2262 – Simvastatin

Simvastatin 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2262

Product details

Brand name
Simvastatin
Generic name
Simvastatin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077691
Marketed since
December 20, 2006
Listing expires
December 31, 2027
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Simvastatin →

Package NDC codes (4)

Package NDCDescriptionSince
71335-2262-130 TABLET, FILM COATED in 1 BOTTLE (71335-2262-1)Apr 3, 2024
71335-2262-290 TABLET, FILM COATED in 1 BOTTLE (71335-2262-2)Oct 10, 2023
71335-2262-360 TABLET, FILM COATED in 1 BOTTLE (71335-2262-3)Apr 3, 2024
71335-2262-410 TABLET, FILM COATED in 1 BOTTLE (71335-2262-4)Apr 3, 2024

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