NDC 68788-8232 – Lovastatin

Lovastatin 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8232

Product details

Brand name
Lovastatin
Generic name
Lovastatin
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078296
Marketed since
August 8, 2022
Listing expires
December 31, 2027
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lovastatin →

Package NDC codes (1)

Package NDCDescriptionSince
68788-8232-330 TABLET in 1 BOTTLE (68788-8232-3)Aug 8, 2022

Other Lovastatin products