Gemfibrozil

NDC 70771-1431 · Zydus Lifesciences Limited

Generic nameGemfibrozil

Dosage formTABLET

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

70771-1431-0 1000 TABLET in 1 BOTTLE (70771-1431-0)

70771-1431-1 100 TABLET in 1 BOTTLE (70771-1431-1)

70771-1431-3 30 TABLET in 1 BOTTLE (70771-1431-3)

70771-1431-4 10 BLISTER PACK in 1 CARTON (70771-1431-4) / 10 TABLET in 1 BLISTER PACK

70771-1431-5 500 TABLET in 1 BOTTLE (70771-1431-5)

70771-1431-6 60 TABLET in 1 BOTTLE (70771-1431-6)

70771-1431-9 90 TABLET in 1 BOTTLE (70771-1431-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65862-624 — Gemfibrozil, 66267-436 — Gemfibrozil, 67046-0233 — Gemfibrozil, 68071-1733 — Gemfibrozil, 68071-2387 — Gemfibrozil, 68382-553 — Gemfibrozil, 68788-7964 — Gemfibrozil, 69097-821 — Gemfibrozil, 70518-1563 — Gemfibrozil, 70518-4305 — Gemfibrozil, 71209-008 — Gemfibrozil, 71335-0051 — GEMFIBROZIL, 71335-1902 — Gemfibrozil, 71335-1996 — Gemfibrozil, 71335-2025 — Gemfibrozil, 71610-107 — Gemfibrozil, 71610-200 — Gemfibrozil, 71610-601 — Gemfibrozil, 71610-824 — Gemfibrozil, 72162-2119 — 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.