OXYCODONE 2.5 Drug Patent Profile
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Which patents cover Oxycodone 2.5, and when can generic versions of Oxycodone 2.5 launch?
Oxycodone 2.5 is a drug marketed by Bristol Myers Squibb and is included in one NDA.
The generic ingredient in OXYCODONE 2.5 is acetaminophen; oxycodone hydrochloride. There are sixty-six drug master file entries for this compound. Thirty suppliers are listed for this compound. Additional details are available on the acetaminophen; oxycodone hydrochloride profile page.
US Patents and Regulatory Information for OXYCODONE 2.5
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Bristol Myers Squibb | OXYCODONE 2.5/APAP 500 | acetaminophen; oxycodone hydrochloride | TABLET;ORAL | 085910-001 | Approved Prior to Jan 1, 1982 | 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 |
