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Last Updated: April 26, 2024

Thioridazine - Generic Drug Details


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What are the generic drug sources for thioridazine and what is the scope of patent protection?

Thioridazine is the generic ingredient in four branded drugs marketed by Novartis, Actavis Mid Atlantic, Alpharma Us Pharms, Ani Pharms, Epic Pharma Llc, Pharm Assoc, Sandoz, Wockhardt, Roxane, Chartwell Rx, Heritage Pharma Avet, Mutual Pharm, Mylan, Par Pharm, Sun Pharm Industries, Superpharm, Watson Labs, Watson Labs Teva, and West Ward, and is included in eighty-one NDAs. Additional information is available in the individual branded drug profile pages.

There are eighteen drug master file entries for thioridazine.

Drug Prices for thioridazine

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Recent Clinical Trials for thioridazine

Identify potential brand extensions & 505(b)(2) entrants

SponsorPhase
Rabin Medical CenterEarly Phase 1
Rambam Health Care CampusEarly Phase 1
State University of New York at BuffaloPhase 4

See all thioridazine clinical trials

Medical Subject Heading (MeSH) Categories for thioridazine

US Patents and Regulatory Information for thioridazine

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Roxane THIORIDAZINE HYDROCHLORIDE thioridazine hydrochloride TABLET;ORAL 088665-001 Mar 15, 1984 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Mylan THIORIDAZINE HYDROCHLORIDE thioridazine hydrochloride TABLET;ORAL 088332-001 Jun 27, 1983 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Sun Pharm Industries THIORIDAZINE HYDROCHLORIDE thioridazine hydrochloride TABLET;ORAL 089953-001 Oct 7, 1988 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Ani Pharms THIORIDAZINE HYDROCHLORIDE thioridazine hydrochloride TABLET;ORAL 088271-001 Apr 14, 1983 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
West Ward THIORIDAZINE HYDROCHLORIDE thioridazine hydrochloride TABLET;ORAL 088659-001 Mar 26, 1984 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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