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Last Updated: April 23, 2024

Prochlorperazine maleate - Generic Drug Details


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What are the generic sources for prochlorperazine maleate and what is the scope of freedom to operate?

Prochlorperazine maleate is the generic ingredient in four branded drugs marketed by Glaxosmithkline, Watson Labs, Amneal, Bionpharma, Chartwell Rx, Duramed Pharms Barr, Glenmark Pharms Ltd, Ivax Sub Teva Pharms, Mylan, Novitium Pharma, Teva Pharms, Zydus, and Jubilant Cadista, and is included in twenty NDAs. Additional information is available in the individual branded drug profile pages.

There are eight drug master file entries for prochlorperazine maleate. Twenty-one suppliers are listed for this compound.

Drug Prices for prochlorperazine maleate

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Drug Sales Revenue Trends for prochlorperazine maleate

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Pharmacology for prochlorperazine maleate
Drug ClassPhenothiazine

US Patents and Regulatory Information for prochlorperazine maleate

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Mylan PROCHLORPERAZINE MALEATE prochlorperazine maleate TABLET;ORAL 040185-001 Oct 28, 1996 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Duramed Pharms Barr PROCHLORPERAZINE MALEATE prochlorperazine maleate TABLET;ORAL 040207-001 May 1, 1997 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Watson Labs PROCHLORPERAZINE prochlorperazine maleate TABLET;ORAL 085580-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Zydus PROCHLORPERAZINE MALEATE prochlorperazine maleate TABLET;ORAL 216495-002 Aug 8, 2022 AB RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Teva Pharms PROCHLORPERAZINE MALEATE prochlorperazine maleate TABLET;ORAL 040120-001 Jul 11, 1996 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Amneal PROCHLORPERAZINE MALEATE prochlorperazine maleate TABLET;ORAL 216598-002 Apr 17, 2023 AB RX 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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