NDC 68788-7964 – Gemfibrozil

Gemfibrozil 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-7964

Product details

Brand name
Gemfibrozil
Generic name
Gemfibrozil
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214603
Marketed since
July 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
68788-7964-330 TABLET in 1 BOTTLE (68788-7964-3)Jul 20, 2021
68788-7964-660 TABLET in 1 BOTTLE (68788-7964-6)Jul 20, 2021
68788-7964-990 TABLET in 1 BOTTLE (68788-7964-9)Jul 20, 2021

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