PHENDIMETRAZINE Drug Patent Profile
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Which patents cover Phendimetrazine, and what generic alternatives are available?
Phendimetrazine is a drug marketed by Acertis Pharms, Graham Dm, Virtus, Sandoz, Vitarine, Barr, Chartwell, Chartwell Rx, Elite Labs Inc, Ferndale Labs, Inwood Labs, Ivax Pharms, Ivax Sub Teva Pharms, Kv Pharm, Kvk Tech, Mfg Chemists, Mpp Pharma, Nexgen Pharma Inc, Numark, Pvt Form, Solvay, Upsher Smith Labs, Usl Pharma, and Watson Labs. and is included in sixty-five NDAs.
The generic ingredient in PHENDIMETRAZINE is phendimetrazine tartrate. There are five drug master file entries for this compound. Twelve suppliers are listed for this compound. Additional details are available on the phendimetrazine tartrate profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Phendimetrazine
A generic version of PHENDIMETRAZINE was approved as phendimetrazine tartrate by CHARTWELL on October 30th, 1991.
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Summary for PHENDIMETRAZINE
| US Patents: | 0 |
| Applicants: | 24 |
| NDAs: | 65 |
| Drug Prices: | Drug price information for PHENDIMETRAZINE |
| DailyMed Link: | PHENDIMETRAZINE at DailyMed |
US Patents and Regulatory Information for PHENDIMETRAZINE
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Kv Pharm | PHENDIMETRAZINE TARTRATE | phendimetrazine tartrate | TABLET;ORAL | 084141-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Ferndale Labs | PHENDIMETRAZINE TARTRATE | phendimetrazine tartrate | TABLET;ORAL | 086834-001 | Sep 15, 1983 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Pvt Form | PHENDIMETRAZINE TARTRATE | phendimetrazine tartrate | TABLET;ORAL | 085697-001 | 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 |
