Gemfibrozil

NDC 50090-7233 · A-S Medication Solutions

Generic nameGemfibrozil

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)GEMFIBROZIL

Strength600 mg/1

Pharmacologic classPPAR alpha [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]

Marketing categoryANDA

Packages

50090-7233-0 — 60 TABLET, FILM COATED in 1 BOTTLE (50090-7233-0)

50090-7233-2 — 90 TABLET, FILM COATED in 1 BOTTLE (50090-7233-2)

50090-7233-3 — 30 TABLET, FILM COATED in 1 BOTTLE (50090-7233-3)

50090-7233-4 — 180 TABLET, FILM COATED in 1 BOTTLE (50090-7233-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0071-0737 — gemfibrozil, 0615-8354 — Gemfibrozil, 16571-784 — Gemfibrozil, 16714-101 — gemfibrozil, 31722-128 — Gemfibrozil, 43063-745 — Gemfibrozil, 50090-5808 — Gemfibrozil, 50090-6913 — gemfibrozil, 50090-6939 — gemfibrozil, 50090-7234 — Gemfibrozil, 50090-7809 — Gemfibrozil, 50268-350 — Gemfibrozil, 51655-143 — Gemfibrozil, 60687-224 — Gemfibrozil, 62135-160 — Gemfibrozil, 63187-772 — Gemfibrozil, 65862-624 — Gemfibrozil, 66267-436 — Gemfibrozil, 67046-0233 — Gemfibrozil, 68071-1733 — Gemfibrozil, +23 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.