NDC 70518-2009 – Lovastatin

Lovastatin 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-2009

Product details

Brand name
Lovastatin
Generic name
Lovastatin
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078296
Marketed since
April 11, 2019
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
70518-2009-090 TABLET in 1 BOTTLE, PLASTIC (70518-2009-0)Apr 11, 2019
70518-2009-130 TABLET in 1 BLISTER PACK (70518-2009-1)Oct 26, 2021

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