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Last Updated: November 4, 2024

Prazosin hydrochloride - Generic Drug Details


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What are the generic sources for prazosin hydrochloride and what is the scope of freedom to operate?

Prazosin hydrochloride is the generic ingredient in three branded drugs marketed by Pfizer, Alembic, Am Therap, Ani Pharms, Appco, Aurobindo Pharma Ltd, Dava Pharms Inc, Granules, Lannett Co Inc, Mankind Pharma, MSN, Mylan, Novitium Pharma, Purepac Pharm, Teva Pharms, and Watson Labs, and is included in twenty-five NDAs. Additional information is available in the individual branded drug profile pages.

There are fourteen drug master file entries for prazosin hydrochloride. Thirty suppliers are listed for this compound.

Summary for prazosin hydrochloride
US Patents:0
Tradenames:3
Applicants:16
NDAs:25
Drug Master File Entries: 14
Finished Product Suppliers / Packagers: 30
Raw Ingredient (Bulk) Api Vendors: 117
Clinical Trials: 67
Patent Applications: 2,629
What excipients (inactive ingredients) are in prazosin hydrochloride?prazosin hydrochloride excipients list
DailyMed Link:prazosin hydrochloride at DailyMed
Recent Clinical Trials for prazosin hydrochloride

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

SponsorPhase
Kinnov TherapeuticsPhase 1
The Royal's Institute of Mental Health ResearchEarly Phase 1
Ottawa Hospital Research InstituteEarly Phase 1

See all prazosin hydrochloride clinical trials

Pharmacology for prazosin hydrochloride
Medical Subject Heading (MeSH) Categories for prazosin hydrochloride

US Patents and Regulatory Information for prazosin hydrochloride

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Novitium Pharma PRAZOSIN HYDROCHLORIDE prazosin hydrochloride CAPSULE;ORAL 210971-001 Oct 3, 2018 AB RX No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Watson Labs PRAZOSIN HYDROCHLORIDE prazosin hydrochloride CAPSULE;ORAL 072609-001 May 16, 1989 DISCN No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Granules PRAZOSIN HYDROCHLORIDE prazosin hydrochloride CAPSULE;ORAL 214608-003 Dec 23, 2021 AB RX No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Purepac Pharm PRAZOSIN HYDROCHLORIDE prazosin hydrochloride CAPSULE;ORAL 072921-001 May 16, 1989 DISCN No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

Expired US Patents for prazosin hydrochloride

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Pfizer MINIPRESS prazosin hydrochloride CAPSULE;ORAL 017442-001 Approved Prior to Jan 1, 1982 ⤷  Sign Up ⤷  Sign Up
Pfizer MINIPRESS XL prazosin hydrochloride TABLET, EXTENDED RELEASE;ORAL 019775-002 Jan 29, 1992 ⤷  Sign Up ⤷  Sign Up
Pfizer MINIPRESS XL prazosin hydrochloride TABLET, EXTENDED RELEASE;ORAL 019775-001 Jan 29, 1992 ⤷  Sign Up ⤷  Sign Up
Pfizer MINIPRESS prazosin hydrochloride CAPSULE;ORAL 017442-002 Approved Prior to Jan 1, 1982 ⤷  Sign Up ⤷  Sign Up
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration

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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.