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Sulfamethoxazole and Trimethoprim

NDC 85766-015 · Sportpharm LLC

Generic nameSulfamethoxazole and Trimethoprim
Dosage formTABLET
RouteORAL
Active ingredient(s)SULFAMETHOXAZOLE, TRIMETHOPRIM
Strength800; 160 mg/1; mg/1
Pharmacologic classCytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Dihydrofolate Reductase Inhibitor Antibacterial [EPC], Dihydrofolate Reductase Inhibitors [MoA], Organic Cation Transporter 2 Inhibitors [MoA], Sulfonamide Antimicrobial [EPC], Sulfonamides [CS]
Marketing categoryANDA

Packages

85766-015-01 100 TABLET in 1 BOTTLE (85766-015-01)

85766-015-05 500 TABLET in 1 BOTTLE (85766-015-05)

85766-015-06 6 TABLET in 1 BOTTLE (85766-015-06)

85766-015-10 10 TABLET in 1 BOTTLE (85766-015-10)

85766-015-14 14 TABLET in 1 BOTTLE (85766-015-14)

85766-015-20 20 TABLET in 1 BOTTLE (85766-015-20)

85766-015-28 28 TABLET in 1 BOTTLE (85766-015-28)

85766-015-30 30 TABLET in 1 BOTTLE (85766-015-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-3432 — Sulfamethoxazole and Trimethoprim, 70518-3454 — Sulfamethoxazole and Trimethoprim, 70518-4381 — polymyxin b sulfate and trimethoprim sulfate, 70934-544 — Sulfamethoxazole and Trimethoprim, 70954-258 — Sulfamethoxazole and Trimethoprim, 70954-541 — Trimethoprim, 71205-810 — Sulfamethoxazole and Trimethoprim, 71335-0762 — Sulfamethoxazole and Trimethoprim, 72789-018 — Sulfamethoxazole and Trimethoprim, 72789-064 — Sulfamethoxazole and Trimethoprim, 75907-043 — Trimethoprim, 76420-064 — Sulfamethoxazole and Trimethoprim, 80425-0001 — Sulfamethoxazole and Trimethoprim, 80425-0002 — Sulfamethoxazole and Trimethoprim, 80425-0003 — Sulfamethoxazole and Trimethoprim, 81033-012 — Sulfamethoxazole and Trimethoprim, 82868-092 — Sulfamethoxazole and Trimethoprim, 82982-044 — Sulfamethoxazole and Trimethoprim, 83939-0023 — Sulfamethoxazole and Trimethoprim, 87441-078 — Sulfamethoxazole and Trimethoprim, +87 more

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