NDC 43063-692 – Lovastatin

Lovastatin 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC43063-692

Product details

Brand name
Lovastatin
Generic name
Lovastatin
Labeler
PD-Rx Pharmaceuticals, Inc.
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 (4)

Package NDCDescriptionSince
43063-692-3030 TABLET in 1 BOTTLE, PLASTIC (43063-692-30)Jul 31, 2023
43063-692-9090 TABLET in 1 BOTTLE, PLASTIC (43063-692-90)Jul 26, 2016
43063-692-93180 TABLET in 1 BOTTLE, PLASTIC (43063-692-93)Jul 26, 2016
43063-692-951000 TABLET in 1 BOTTLE, PLASTIC (43063-692-95)Oct 3, 2022

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