NDC 71335-9636 – Simvastatin

Simvastatin 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-9636

Product details

Brand name
Simvastatin
Generic name
Simvastatin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078103
Marketed since
June 12, 2007
Listing expires
December 31, 2027
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Simvastatin →

Package NDC codes (7)

Package NDCDescriptionSince
71335-9636-130 TABLET, FILM COATED in 1 BOTTLE (71335-9636-1)Mar 13, 2023
71335-9636-290 TABLET, FILM COATED in 1 BOTTLE (71335-9636-2)Mar 3, 2023
71335-9636-3120 TABLET, FILM COATED in 1 BOTTLE (71335-9636-3)Apr 3, 2024
71335-9636-4100 TABLET, FILM COATED in 1 BOTTLE (71335-9636-4)Oct 19, 2023
71335-9636-560 TABLET, FILM COATED in 1 BOTTLE (71335-9636-5)Apr 3, 2024
71335-9636-628 TABLET, FILM COATED in 1 BOTTLE (71335-9636-6)Apr 3, 2024
71335-9636-710 TABLET, FILM COATED in 1 BOTTLE (71335-9636-7)Apr 3, 2024

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