NDC 63629-1018 – Lovastatin

Lovastatin 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63629-1018

Product details

Brand name
Lovastatin
Generic name
Lovastatin
Labeler
Bryant Ranch Prepack
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 (9)

Package NDCDescriptionSince
63629-1018-01000 TABLET in 1 BOTTLE (63629-1018-0)Aug 14, 2024
63629-1018-1100 TABLET in 1 BOTTLE (63629-1018-1)Aug 14, 2024
63629-1018-230 TABLET in 1 BOTTLE (63629-1018-2)Aug 14, 2024
63629-1018-3300 TABLET in 1 BOTTLE (63629-1018-3)Aug 14, 2024
63629-1018-4120 TABLET in 1 BOTTLE (63629-1018-4)Dec 16, 2019
63629-1018-5500 TABLET in 1 BOTTLE (63629-1018-5)Dec 10, 2019
63629-1018-660 TABLET in 1 BOTTLE (63629-1018-6)Aug 14, 2024
63629-1018-8800 TABLET in 1 BOTTLE (63629-1018-8)Aug 14, 2024
63629-1018-990 TABLET in 1 BOTTLE (63629-1018-9)Aug 14, 2024

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