NDC 50090-3881 – Lovastatin

Lovastatin 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50090-3881

Product details

Brand name
Lovastatin
Generic name
Lovastatin
Labeler
A-S Medication Solutions
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 (2)

Package NDCDescriptionSince
50090-3881-030 TABLET in 1 BOTTLE (50090-3881-0)Nov 28, 2018
50090-3881-290 TABLET in 1 BOTTLE, PLASTIC (50090-3881-2)Nov 28, 2014

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