Gemfibrozil

NDC 71335-1902 · Bryant Ranch Prepack

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

71335-1902-1 — 60 TABLET in 1 BOTTLE (71335-1902-1)

71335-1902-2 — 30 TABLET in 1 BOTTLE (71335-1902-2)

71335-1902-3 — 100 TABLET in 1 BOTTLE (71335-1902-3)

71335-1902-4 — 90 TABLET in 1 BOTTLE (71335-1902-4)

71335-1902-5 — 180 TABLET in 1 BOTTLE (71335-1902-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-1733 — Gemfibrozil, 68071-2387 — 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, 71335-1996 — Gemfibrozil, 71335-2025 — Gemfibrozil, 71610-107 — Gemfibrozil, 71610-200 — Gemfibrozil, 71610-601 — Gemfibrozil, 71610-824 — Gemfibrozil, 72162-2119 — Gemfibrozil, 72578-066 — Gemfibrozil, 72603-206 — Gemfibrozil, 72865-186 — 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.