NDC 71335-1905 – Simvastatin

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

Human Prescription Drug

Product NDC71335-1905

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 (7)

Package NDCDescriptionSince
71335-1905-130 TABLET, FILM COATED in 1 BOTTLE (71335-1905-1)Sep 8, 2021
71335-1905-290 TABLET, FILM COATED in 1 BOTTLE (71335-1905-2)Sep 13, 2021
71335-1905-3120 TABLET, FILM COATED in 1 BOTTLE (71335-1905-3)Dec 29, 2021
71335-1905-4100 TABLET, FILM COATED in 1 BOTTLE (71335-1905-4)Jul 19, 2021
71335-1905-560 TABLET, FILM COATED in 1 BOTTLE (71335-1905-5)Dec 29, 2021
71335-1905-628 TABLET, FILM COATED in 1 BOTTLE (71335-1905-6)Dec 29, 2021
71335-1905-710 TABLET, FILM COATED in 1 BOTTLE (71335-1905-7)Dec 29, 2021

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