NDC 68071-2387 – Gemfibrozil

Gemfibrozil 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-2387

Product details

Brand name
Gemfibrozil
Generic name
Gemfibrozil
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214603
Marketed since
January 20, 2021
Listing expires
December 31, 2027
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist

Active ingredients

Uses, dosage, side effects and warnings for Gemfibrozil →

Package NDC codes (3)

Package NDCDescriptionSince
68071-2387-330 TABLET in 1 BOTTLE (68071-2387-3)Apr 13, 2021
68071-2387-660 TABLET in 1 BOTTLE (68071-2387-6)Apr 13, 2021
68071-2387-8180 TABLET in 1 BOTTLE (68071-2387-8)Apr 13, 2021

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