GEMFIBROZIL

NDC 68071-2387 · NuCare Pharmaceuticals,Inc.

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

68071-2387-3 — 30 TABLET in 1 BOTTLE (68071-2387-3)

68071-2387-6 — 60 TABLET in 1 BOTTLE (68071-2387-6)

68071-2387-8 — 180 TABLET in 1 BOTTLE (68071-2387-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 68382-553 — Gemfibrozil, 68788-7964 — Gemfibrozil, 69097-821 — Gemfibrozil, 70518-1563 — Gemfibrozil, 70518-4305 — Gemfibrozil, 70771-1431 — Gemfibrozil, 71209-008 — Gemfibrozil, 71335-0051 — GEMFIBROZIL, 71335-1902 — Gemfibrozil, 71335-1996 — 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.