NDC 63629-1464 – Lovastatin

Lovastatin 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63629-1464

Product details

Brand name
Lovastatin
Generic name
Lovastatin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075991
Marketed since
November 25, 2002
Listing expires
December 31, 2026
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lovastatin →

Package NDC codes (5)

Package NDCDescriptionSince
63629-1464-130 TABLET in 1 BOTTLE (63629-1464-1)Jan 26, 2005
63629-1464-2100 TABLET in 1 BOTTLE (63629-1464-2)Sep 30, 2009
63629-1464-360 TABLET in 1 BOTTLE (63629-1464-3)Jan 19, 2009
63629-1464-490 TABLET in 1 BOTTLE (63629-1464-4)Jun 12, 2012
63629-1464-520 TABLET in 1 BOTTLE (63629-1464-5)Dec 26, 2018

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