FDA Orange Book
Is there a generic for Technegas Kit?
Technegas Kit contains technetium tc-99m labeled carbon. 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 Technegas Kit (technetium tc-99m labeled carbon). The Orange Book shows its last listed patent expires February 24, 2031 and its last listed exclusivity ends September 29, 2026.
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Technegas Kit products in the Orange Book
| Form and route | Strength | Brand status | Brand TE | Active generics | Generic TE codes |
|---|---|---|---|---|---|
| aerosol, inhalation | N/A | Marketed (Rx) | None | 0 | None |
NDA 022335, held by CYCLOMEDICA AUSTRALIA PTY LTD. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.
Technegas Kit patents
| Patent | Expires | Covers | Use code | NDA |
|---|---|---|---|---|
| 7722856 | February 24, 2031 | Method of use | U-4442 | 022335 |
Technegas Kit exclusivity
| Code | Meaning | Expires | NDA |
|---|---|---|---|
| NP | New product | September 29, 2026 | 022335 |
Questions
Is there a generic for Technegas Kit?
No. The Orange Book lists no active FDA-approved generic (ANDA) for Technegas Kit (technetium tc-99m labeled carbon). The Orange Book shows its last listed patent expires February 24, 2031 and its last listed exclusivity ends September 29, 2026.
What is the generic name for Technegas Kit?
The active ingredient in Technegas Kit is technetium tc-99m labeled carbon, per the FDA Orange Book.
When does the Technegas Kit patent expire?
The last patent listed for Technegas Kit in the Orange Book expires February 24, 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.