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Last Updated: March 18, 2024

THIORIDAZINE HYDROCHLORIDE - Generic Drug Details


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

Thioridazine hydrochloride is the generic ingredient in three 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 NDAs. Additional information is available in the individual branded drug profile pages.

There are six drug master file entries for thioridazine hydrochloride. Three suppliers are listed for this compound.

Summary for THIORIDAZINE HYDROCHLORIDE
Recent Clinical Trials for THIORIDAZINE HYDROCHLORIDE

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 HYDROCHLORIDE clinical trials

Pharmacology for THIORIDAZINE HYDROCHLORIDE
Drug ClassPhenothiazine

US Patents and Regulatory Information for THIORIDAZINE HYDROCHLORIDE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Par Pharm THIORIDAZINE HYDROCHLORIDE thioridazine hydrochloride TABLET;ORAL 088336-001 Dec 5, 1983 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Novartis MELLARIL thioridazine hydrochloride TABLET;ORAL 011808-003 Approved Prior to Jan 1, 1982 DISCN Yes No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Par Pharm THIORIDAZINE HYDROCHLORIDE thioridazine hydrochloride TABLET;ORAL 088351-001 Dec 5, 1983 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Novartis MELLARIL thioridazine hydrochloride TABLET;ORAL 011808-017 Approved Prior to Jan 1, 1982 DISCN Yes 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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