NDC 71335-9642 – Simvastatin

Simvastatin 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-9642

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 14, 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 (8)

Package NDCDescriptionSince
71335-9642-130 TABLET, FILM COATED in 1 BOTTLE (71335-9642-1)Feb 27, 2023
71335-9642-260 TABLET, FILM COATED in 1 BOTTLE (71335-9642-2)Feb 27, 2023
71335-9642-3100 TABLET, FILM COATED in 1 BOTTLE (71335-9642-3)Mar 3, 2025
71335-9642-490 TABLET, FILM COATED in 1 BOTTLE (71335-9642-4)Feb 17, 2023
71335-9642-5120 TABLET, FILM COATED in 1 BOTTLE (71335-9642-5)Mar 12, 2025
71335-9642-6180 TABLET, FILM COATED in 1 BOTTLE (71335-9642-6)Apr 15, 2026
71335-9642-73 TABLET, FILM COATED in 1 BOTTLE (71335-9642-7)Apr 15, 2026
71335-9642-810 TABLET, FILM COATED in 1 BOTTLE (71335-9642-8)Apr 15, 2026

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