NDC 68180-467 – Lovastatin

Lovastatin 10 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC68180-467

Product details

Brand name
Lovastatin
Generic name
lovastatin
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078296
Marketed since
March 14, 2008
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
68180-467-01100 TABLET in 1 BOTTLE (68180-467-01)Mar 14, 2008
68180-467-031000 TABLET in 1 BOTTLE (68180-467-03)Mar 14, 2008
68180-467-0760 TABLET in 1 BOTTLE (68180-467-07)Mar 14, 2008
68180-467-0990 TABLET in 1 BOTTLE (68180-467-09)Jun 4, 2019

Recalls mentioning this NDC

Other Lovastatin products