NDC 71205-199 – Lovastatin

Lovastatin 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-199

Product details

Brand name
Lovastatin
Generic name
Lovastatin
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078296
Marketed since
November 1, 2007
Listing expires
December 31, 2026
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lovastatin →

Package NDC codes (3)

Package NDCDescriptionSince
71205-199-3030 TABLET in 1 BOTTLE (71205-199-30)Jan 1, 2019
71205-199-6060 TABLET in 1 BOTTLE (71205-199-60)Jan 1, 2019
71205-199-9090 TABLET in 1 BOTTLE (71205-199-90)Jan 1, 2019

Other Lovastatin products