FDA Orange Book

Generic for Septra DS

Septra DS contains sulfamethoxazole and trimethoprim. Orange Book status for every listed strength, the approved generic makers, and the listed patents and exclusivities.

Source: FDA Orange Book data file dated 2026-10-09. Publisher page

Yes. The generic name for Septra DS is sulfamethoxazole and trimethoprim. 6 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB.

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Septra DS products in the Orange Book

Septra DS products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
tablet, oral800MG;160MGDiscontinuedNone6AB

NDA 017376, held by MONARCH PHARMACEUTICALS LLC. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

Approved generic sulfamethoxazole and trimethoprim

Approved generic versions of Septra DS
CompanyANDATE codeApprovedStrengths
SUN PHARMACEUTICAL INDUSTRIES INC071017AB (A-rated, therapeutically equivalent)August 25, 1986800MG;160MG
AMNEAL PHARMACEUTICALS NY LLC076899AB (A-rated, therapeutically equivalent)January 27, 2005800MG;160MG
VISTA PHARMACEUTICALS INC076817AB (A-rated, therapeutically equivalent)October 7, 2005800MG;160MG
CHARTWELL MOLECULES LLC078060AB (A-rated, therapeutically equivalent)January 25, 2007800MG;160MG
AUROBINDO PHARMA LTD090624AB (A-rated, therapeutically equivalent)February 16, 2010800MG;160MG
GLENMARK PHARMACEUTICALS LTD090828AB (A-rated, therapeutically equivalent)December 22, 2010800MG;160MG

Questions

Is there a generic for Septra DS?

Yes. The generic name for Septra DS is sulfamethoxazole and trimethoprim. 6 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB.

What is the generic name for Septra DS?

The active ingredient in Septra DS is sulfamethoxazole and trimethoprim, per the FDA Orange Book.

What does a therapeutic equivalence code mean?

In the Orange Book, codes that start with A (such as AB) mean FDA considers the product therapeutically equivalent to the reference drug. Codes that start with B mean FDA does not, at this time, consider the product therapeutically equivalent.

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