NDC 68180-468 – Lovastatin

Lovastatin 20 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC68180-468

Product details

Brand name
Lovastatin
Generic name
Lovastatin
Labeler
Lupin Pharmaceuticals, Inc.
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 (4)

Package NDCDescriptionSince
68180-468-01100 TABLET in 1 BOTTLE (68180-468-01)Nov 1, 2007
68180-468-031000 TABLET in 1 BOTTLE (68180-468-03)Nov 1, 2007
68180-468-055000 TABLET in 1 BOTTLE (68180-468-05)Nov 1, 2007
68180-468-0760 TABLET in 1 BOTTLE (68180-468-07)Nov 1, 2007

Recalls mentioning this NDC

Other Lovastatin products