NDC 68788-7056 – Lovastatin

Lovastatin 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-7056

Product details

Brand name
Lovastatin
Generic name
Lovastatin
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075991
Marketed since
January 5, 2018
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
68788-7056-1100 TABLET in 1 BOTTLE (68788-7056-1)Jan 5, 2018
68788-7056-330 TABLET in 1 BOTTLE (68788-7056-3)Jan 5, 2018
68788-7056-660 TABLET in 1 BOTTLE (68788-7056-6)Jan 5, 2018
68788-7056-990 TABLET in 1 BOTTLE (68788-7056-9)Jan 5, 2018

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