NDC 71205-994 – Lovastatin

Lovastatin 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-994

Product details

Brand name
Lovastatin
Generic name
Lovastatin
Labeler
Proficient Rx LP
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 (6)

Package NDCDescriptionSince
71205-994-00100 TABLET in 1 BOTTLE (71205-994-00)Apr 1, 2020
71205-994-111000 TABLET in 1 BOTTLE (71205-994-11)Apr 1, 2020
71205-994-3030 TABLET in 1 BOTTLE (71205-994-30)Apr 1, 2020
71205-994-55500 TABLET in 1 BOTTLE (71205-994-55)Apr 1, 2020
71205-994-6060 TABLET in 1 BOTTLE (71205-994-60)Apr 1, 2020
71205-994-9090 TABLET in 1 BOTTLE (71205-994-90)Apr 1, 2020

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