FDA Orange Book

Is there a generic for iDose TR?

iDose TR contains travoprost. 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

No. The Orange Book lists no active FDA-approved generic (ANDA) for iDose TR (travoprost). The Orange Book shows its last listed patent expires February 14, 2031 and its last listed exclusivity ends December 13, 2026.

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iDose TR products in the Orange Book

iDose TR products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
implant, intracameral75MCGMarketed (Rx)None0None

NDA 218010, held by GLAUKOS CORP. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

iDose TR patents

Patents listed for iDose TR
PatentExpiresCoversUse codeNDA
12201557June 18, 2030Drug substance, Drug productU-4129218010
11426306October 17, 2030Drug productNone218010
10206813October 17, 2030Drug productNone218010
12201555February 14, 2031Drug substance, Drug productNone218010

iDose TR exclusivity

Exclusivity listed for iDose TR
CodeMeaningExpiresNDA
NPNew productDecember 13, 2026218010

iDose TR NDC codes

Questions

Is there a generic for iDose TR?

No. The Orange Book lists no active FDA-approved generic (ANDA) for iDose TR (travoprost). The Orange Book shows its last listed patent expires February 14, 2031 and its last listed exclusivity ends December 13, 2026.

What is the generic name for iDose TR?

The active ingredient in iDose TR is travoprost, per the FDA Orange Book.

When does the iDose TR patent expire?

The last patent listed for iDose TR in the Orange Book expires February 14, 2031. A listed patent expiry date is not a generic launch date.

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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