ibuprofen; oxycodone hydrochloride - Profile
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What are the generic sources for ibuprofen; oxycodone hydrochloride and what is the scope of patent protection?
Ibuprofen; oxycodone hydrochloride
is the generic ingredient in two branded drugs marketed by Forest Labs, Actavis Elizabeth, Barr Labs Inc, and Watson Labs, and is included in four NDAs. Additional information is available in the individual branded drug profile pages.Summary for ibuprofen; oxycodone hydrochloride
| US Patents: | 0 |
| Tradenames: | 2 |
| Applicants: | 4 |
| NDAs: | 4 |
US Patents and Regulatory Information for ibuprofen; oxycodone hydrochloride
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Forest Labs | COMBUNOX | ibuprofen; oxycodone hydrochloride | TABLET;ORAL | 021378-001 | Nov 26, 2004 | DISCN | Yes | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Actavis Elizabeth | OXYCODONE HYDROCHLORIDE AND IBUPROFEN | ibuprofen; oxycodone hydrochloride | TABLET;ORAL | 078769-001 | Jan 4, 2008 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Barr Labs Inc | OXYCODONE HYDROCHLORIDE AND IBUPROFEN | ibuprofen; oxycodone hydrochloride | TABLET;ORAL | 078316-001 | Nov 29, 2007 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |
Expired US Patents for ibuprofen; oxycodone hydrochloride
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Patent No. | Patent Expiration |
|---|---|---|---|---|---|---|---|
| Forest Labs | COMBUNOX | ibuprofen; oxycodone hydrochloride | TABLET;ORAL | 021378-001 | Nov 26, 2004 | 4,569,937 | ⤷ Start Trial |
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >Patent No. | >Patent Expiration |
