NDC 0093-0576 – Lovastatin

Lovastatin 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0093-0576

Product details

Brand name
Lovastatin
Generic name
Lovastatin
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075551
Marketed since
December 17, 2001
Listing expires
December 31, 2026
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lovastatin →

Package NDC codes (2)

Package NDCDescriptionSince
0093-0576-0660 TABLET in 1 BOTTLE (0093-0576-06)Dec 17, 2001
0093-0576-101000 TABLET in 1 BOTTLE (0093-0576-10)Dec 17, 2001

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