# TECHNIVIE — FDA application NDA207931

Informational only - not investment advice.

Application NDA207931 · type NDA · FDA status: approved · original approval 2015-07-24

Listed sponsor: ABBVIE · [ABBV company profile](/company/ABBV/) · exact_unique

Sponsor as listed in Drugs@FDA at retrieval (2026-08-07); FDA sponsor listings can lag ownership transfers.

## FDA application facts

| Product | FDA-listed trade name | Active ingredient | Dosage form | Route | Strength | Marketing status | TE code | RLD |
| --- | --- | --- | --- | --- | --- | --- | --- | --- |
| 001 | TECHNIVIE | OMBITASVIR; PARITAPREVIR; RITONAVIR | TABLET | ORAL | 12.5MG;75MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | Discontinued | not listed | Yes |

## Orange Book patent and exclusivity listings

- Patent 8642538, product 001; listed patent expiry date: 2029-09-10.
- Patent 9006387, product 001; listed patent expiry date: 2030-06-10.
- Patent 8420596, product 001; listed patent expiry date: 2031-04-10.
- Patent 9044480, product 001; listed patent expiry date: 2031-04-10.
- Patent 8686026, product 001; listed patent expiry date: 2031-06-09.
- Patent 8420596, product 001; listed patent expiry date: 2031-10-10.
- Patent 8691938, product 001; listed patent expiry date: 2032-04-13.

Patent and exclusivity dates are regulatory listings from the FDA Orange Book; no relationship to revenue or future sales is stated or implied.

## Compound cross-links

- OMBITASVIR; PARITAPREVIR; RITONAVIR · UNII not resolved · no lmmol compound match

Ingredient–compound links use FDA openFDA/GSRS identifiers and an exact lmmol InChIKey join. Ingredient names cannot create a link.

## Related pages

- [Sponsor company](/company/ABBV/)
- [FDA-approved application index](/drug/)
- [Large-cap biopharma](/compare/pharma/)

Sources: https://www.fda.gov/drugs/drug-approvals-and-databases/drugsfda-data-files · https://www.fda.gov/drugs/drug-approvals-and-databases/orange-book-data-files · https://api.fda.gov/drug/drugsfda.json?search=application_number:NDA207931. FDA data retrieved 2026-08-07.

Regulatory listing data as published by FDA; not medical or investment advice.