NDC 71335-1891 – Simvastatin

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

Human Prescription Drug

Product NDC71335-1891

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
71335-1891-130 TABLET, FILM COATED in 1 BOTTLE (71335-1891-1)Jul 30, 2021
71335-1891-260 TABLET, FILM COATED in 1 BOTTLE (71335-1891-2)Dec 29, 2021
71335-1891-3100 TABLET, FILM COATED in 1 BOTTLE (71335-1891-3)Dec 29, 2021
71335-1891-490 TABLET, FILM COATED in 1 BOTTLE (71335-1891-4)Jun 21, 2021
71335-1891-5120 TABLET, FILM COATED in 1 BOTTLE (71335-1891-5)Dec 29, 2021
71335-1891-6180 TABLET, FILM COATED in 1 BOTTLE (71335-1891-6)Dec 29, 2021
71335-1891-73 TABLET, FILM COATED in 1 BOTTLE (71335-1891-7)Dec 29, 2021
71335-1891-810 TABLET, FILM COATED in 1 BOTTLE (71335-1891-8)Dec 29, 2021

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