Gemfibrozil

NDC 51655-143 · Northwind Health Company, LLC

Generic nameGemfibrozil

Dosage formTABLET

RouteORAL

Active ingredient(s)GEMFIBROZIL

Strength600 mg/1

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

Marketing categoryANDA

Packages

51655-143-25 — 60 TABLET in 1 BOTTLE, PLASTIC (51655-143-25)

51655-143-26 — 90 TABLET in 1 BOTTLE, PLASTIC (51655-143-26)

51655-143-52 — 30 TABLET in 1 BOTTLE, PLASTIC (51655-143-52)

51655-143-83 — 180 TABLET in 1 BOTTLE, PLASTIC (51655-143-83)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

16714-101 — gemfibrozil, 31722-128 — Gemfibrozil, 43063-745 — Gemfibrozil, 50090-5808 — Gemfibrozil, 50090-6913 — gemfibrozil, 50090-6939 — gemfibrozil, 50090-7233 — Gemfibrozil, 50090-7234 — Gemfibrozil, 50090-7809 — Gemfibrozil, 50268-350 — Gemfibrozil, 60687-224 — Gemfibrozil, 62135-160 — Gemfibrozil, 63187-772 — Gemfibrozil, 65862-624 — Gemfibrozil, 66267-436 — Gemfibrozil, 67046-0233 — Gemfibrozil, 68071-1733 — Gemfibrozil, 68071-2387 — Gemfibrozil, 68382-553 — Gemfibrozil, 68788-7964 — 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.