NDC 68071-3261 – Lovastatin

Lovastatin 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3261

Product details

Brand name
Lovastatin
Generic name
Lovastatin
Labeler
NuCare Pharmaceuticals, Inc.
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
68071-3261-330 TABLET in 1 BOTTLE (68071-3261-3)May 22, 2017
68071-3261-660 TABLET in 1 BOTTLE (68071-3261-6)May 22, 2017
68071-3261-990 TABLET in 1 BOTTLE (68071-3261-9)May 22, 2017

Other Lovastatin products