NDC 71335-1906 – Simvastatin

Simvastatin 40 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1906

Product details

Brand name
Simvastatin
Generic name
Simvastatin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078034
Marketed since
December 17, 2015
Listing expires
December 31, 2026
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Simvastatin →

Package NDC codes (8)

Package NDCDescriptionSince
71335-1906-130 TABLET, FILM COATED in 1 BOTTLE (71335-1906-1)Jul 14, 2021
71335-1906-260 TABLET, FILM COATED in 1 BOTTLE (71335-1906-2)Dec 29, 2021
71335-1906-390 TABLET, FILM COATED in 1 BOTTLE (71335-1906-3)Jul 13, 2021
71335-1906-4180 TABLET, FILM COATED in 1 BOTTLE (71335-1906-4)Dec 29, 2021
71335-1906-5100 TABLET, FILM COATED in 1 BOTTLE (71335-1906-5)Sep 29, 2021
71335-1906-6120 TABLET, FILM COATED in 1 BOTTLE (71335-1906-6)Dec 29, 2021
71335-1906-728 TABLET, FILM COATED in 1 BOTTLE (71335-1906-7)Dec 29, 2021
71335-1906-810 TABLET, FILM COATED in 1 BOTTLE (71335-1906-8)Dec 29, 2021

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