NDC 68001-316 – Lovastatin

Lovastatin 40 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC68001-316

Product details

Brand name
Lovastatin
Generic name
Lovastatin
Labeler
BluePoint Laboratories
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 (2)

Package NDCDescriptionSince
68001-316-00100 TABLET in 1 BOTTLE (68001-316-00)Feb 7, 2017
68001-316-081000 TABLET in 1 BOTTLE (68001-316-08)Feb 7, 2017

Recalls mentioning this NDC

Other Lovastatin products