Sulfamethoxazole and Trimethoprim

NDC 0703-9526 · Teva Parenteral Medicines, Inc.

FDA carries 2 listing records for this NDC; the most recent is shown.

Generic nameSulfamethoxazole and Trimethoprim

Dosage formINJECTION, SOLUTION, CONCENTRATE

RouteINTRAVENOUS

Active ingredient(s)SULFAMETHOXAZOLE, TRIMETHOPRIM

Strength80; 16 mg/mL; mg/mL

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

0703-9526-81 — 1 VIAL, MULTI-DOSE in 1 CARTON (0703-9526-81) / 30 mL in 1 VIAL, MULTI-DOSE

0703-9526-01 — 1 VIAL, MULTI-DOSE in 1 CARTON (0703-9526-01) / 30 mL in 1 VIAL, MULTI-DOSE

Billed under HCPCS

J2865 — Injection, sulfamethoxazole 5 mg and trimethoprim 1 mg Medicare Part B payment limit (ASP + 6%): $0.04

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0121-0853 — Sulfamethoxazole and Trimethoprim, 0121-0854 — Sulfamethoxazole and Trimethoprim, 0615-8121 — Sulfamethoxazole and Trimethoprim, 0703-9503 — Sulfamethoxazole and Trimethoprim, 0703-9514 — Sulfamethoxazole and Trimethoprim, 0904-2725 — Sulfamethoxazole and Trimethoprim, 17856-0496 — Sulfamethoxazole and Trimethoprim, 40032-330 — Trimethoprim, 42291-758 — Sulfamethoxazole and Trimethoprim, 42291-759 — Sulfamethoxazole and Trimethoprim, 42708-053 — Sulfamethoxazole and Trimethoprim, 43386-330 — Trimethoprim, 49708-145 — sulfamethoxazole and Trimethoprim, 49708-146 — sulfamethoxazole and Trimethoprim, 50090-0525 — Sulfamethoxazole and Trimethoprim, 50090-2198 — Sulfamethoxazole and Trimethoprim, 50090-2199 — Sulfamethoxazole and Trimethoprim, 50090-2200 — Sulfamethoxazole and Trimethoprim, 50090-2201 — Sulfamethoxazole and Trimethoprim, 50090-2479 — Sulfamethoxazole and Trimethoprim, +87 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.