NDC 71610-775 – Lovastatin

Lovastatin 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-775

Product details

Brand name
Lovastatin
Generic name
Lovastatin
Labeler
Aphena Pharma Solutions - Tennessee, LLC
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 (5)

Package NDCDescriptionSince
71610-775-3030 TABLET in 1 BOTTLE, PLASTIC (71610-775-30)Jan 22, 2024
71610-775-4545 TABLET in 1 BOTTLE, PLASTIC (71610-775-45)Jan 22, 2024
71610-775-5360 TABLET in 1 BOTTLE, PLASTIC (71610-775-53)Jan 22, 2024
71610-775-6090 TABLET in 1 BOTTLE, PLASTIC (71610-775-60)Jan 22, 2024
71610-775-80180 TABLET in 1 BOTTLE, PLASTIC (71610-775-80)Jan 22, 2024

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