NDC 68788-8326 – Lovastatin

Lovastatin 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8326

Product details

Brand name
Lovastatin
Generic name
Lovastatin
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078296
Marketed since
January 19, 2023
Listing expires
December 31, 2027
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lovastatin →

Package NDC codes (4)

Package NDCDescriptionSince
68788-8326-1100 TABLET in 1 BOTTLE (68788-8326-1)Jan 19, 2023
68788-8326-330 TABLET in 1 BOTTLE (68788-8326-3)Jan 19, 2023
68788-8326-660 TABLET in 1 BOTTLE (68788-8326-6)Jan 19, 2023
68788-8326-990 TABLET in 1 BOTTLE (68788-8326-9)Jan 19, 2023

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