FDA Orange Book

Generic for Transderm Scop

Transderm Scop contains scopolamine. 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 Transderm Scop is scopolamine. 7 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB.

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Transderm Scop products in the Orange Book

Transderm Scop products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
system, transdermal1MG/72HRMarketed (Rx)AB7AB

NDA 017874, held by BAXTER HEALTHCARE CORP. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

Approved generic scopolamine

Approved generic versions of Transderm Scop
CompanyANDATE codeApprovedStrengths
PADAGIS US LLC078830AB (A-rated, therapeutically equivalent)January 30, 20151MG/72HR
MYLAN TECHNOLOGIES INC203753AB (A-rated, therapeutically equivalent)June 19, 20191MG/72HR
RICONPHARMA LLC212342AB (A-rated, therapeutically equivalent)November 24, 20201MG/72HR
ACTAVIS LABORATORIES UT INC208769AB (A-rated, therapeutically equivalent)January 10, 20221MG/72HR
RHODES PHARMACEUTICALS LP215329AB (A-rated, therapeutically equivalent)May 6, 20241MG/72HR
ZYDUS PHARMACEUTICALS USA INC217893AB (A-rated, therapeutically equivalent)August 29, 20241MG/72HR
AMNEAL PHARMACEUTICALS LLC218384AB (A-rated, therapeutically equivalent)June 9, 20251MG/72HR

Transderm Scop NDC codes

Questions

Is there a generic for Transderm Scop?

Yes. The generic name for Transderm Scop is scopolamine. 7 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 Transderm Scop?

The active ingredient in Transderm Scop is scopolamine, 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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