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Last Updated: March 19, 2024

Phendimetrazine tartrate - Generic Drug Details


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What are the generic drug sources for phendimetrazine tartrate and what is the scope of freedom to operate?

Phendimetrazine tartrate is the generic ingredient in nineteen branded drugs marketed by Valeant, Numark, Graham Dm, Virtus, Shire Richwood, Mast Mm, Sandoz, Vitarine, Solvay, Teva, Ferndale Labs, Abc Holding, Camall, Chartwell Rx, Pvt Form, Forest Pharms, Barr, Chartwell, Elite Labs Inc, Inwood Labs, Ivax Pharms, Ivax Sub Teva Pharms, Kv Pharm, Kvk Tech, Mfg Chemists, Nexgen Pharma Inc, Nostrum Labs Inc, Upsher Smith Labs, Usl Pharma, Watson Labs, and Wyeth Ayerst, and is included in ninety-six NDAs. Additional information is available in the individual branded drug profile pages.

There are three drug master file entries for phendimetrazine tartrate. Twelve suppliers are listed for this compound.

Summary for phendimetrazine tartrate
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Pharmacology for phendimetrazine tartrate

US Patents and Regulatory Information for phendimetrazine tartrate

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Ivax Sub Teva Pharms PHENDIMETRAZINE TARTRATE phendimetrazine tartrate TABLET;ORAL 083682-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Shire Richwood X-TROZINE phendimetrazine tartrate TABLET;ORAL 086551-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Numark MELFIAT phendimetrazine tartrate TABLET;ORAL 083790-002 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Watson Labs PHENDIMETRAZINE TARTRATE phendimetrazine tartrate TABLET;ORAL 085767-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Teva STATOBEX phendimetrazine tartrate CAPSULE;ORAL 085507-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

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