NDC 61442-142 – Lovastatin

Lovastatin 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC61442-142

Product details

Brand name
Lovastatin
Generic name
Lovastatin
Labeler
Carlsbad Technology, 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
61442-142-01100 TABLET in 1 BOTTLE (61442-142-01)Nov 25, 2002
61442-142-05500 TABLET in 1 BOTTLE (61442-142-05)Nov 25, 2002
61442-142-101000 TABLET in 1 BOTTLE (61442-142-10)Nov 25, 2002
61442-142-6060 TABLET in 1 BOTTLE (61442-142-60)Nov 25, 2002

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