NDC 68788-9668 – Lovastatin

Lovastatin 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-9668

Product details

Brand name
Lovastatin
Generic name
Lovastatin
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075991
Marketed since
July 29, 2013
Listing expires
December 31, 2027
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lovastatin →

Package NDC codes (4)

Package NDCDescriptionSince
68788-9668-1100 TABLET in 1 BOTTLE (68788-9668-1)Jul 29, 2013
68788-9668-330 TABLET in 1 BOTTLE (68788-9668-3)Jul 29, 2013
68788-9668-660 TABLET in 1 BOTTLE (68788-9668-6)Jul 29, 2013
68788-9668-990 TABLET in 1 BOTTLE (68788-9668-9)Jul 29, 2013

Other Lovastatin products