NDC 71335-0819 – Lovastatin

Lovastatin 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0819

Product details

Brand name
Lovastatin
Generic name
Lovastatin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078296
Marketed since
November 1, 2007
Listing expires
December 31, 2027
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lovastatin →

Package NDC codes (5)

Package NDCDescriptionSince
71335-0819-130 TABLET in 1 BOTTLE (71335-0819-1)May 8, 2018
71335-0819-2100 TABLET in 1 BOTTLE (71335-0819-2)Apr 4, 2024
71335-0819-360 TABLET in 1 BOTTLE (71335-0819-3)Apr 4, 2024
71335-0819-490 TABLET in 1 BOTTLE (71335-0819-4)Jun 22, 2018
71335-0819-520 TABLET in 1 BOTTLE (71335-0819-5)Apr 4, 2024

Other Lovastatin products