NDC 68071-3615 – Lovastatin

Lovastatin 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3615

Product details

Brand name
Lovastatin
Generic name
lovastatin
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078296
Marketed since
November 1, 2007
Listing expires
December 31, 2026
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lovastatin →

Package NDC codes (1)

Package NDCDescriptionSince
68071-3615-1100 TABLET in 1 BOTTLE (68071-3615-1)May 30, 2024

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