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Last Updated: March 18, 2024

PRIMAQUINE PHOSPHATE Drug Patent Profile


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Which patents cover Primaquine Phosphate, and when can generic versions of Primaquine Phosphate launch?

Primaquine Phosphate is a drug marketed by Alvogen, Bayshore Pharms Llc, and Novast Labs. and is included in three NDAs.

The generic ingredient in PRIMAQUINE PHOSPHATE is primaquine phosphate. There are four drug master file entries for this compound. Six suppliers are listed for this compound. Additional details are available on the primaquine phosphate profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Primaquine Phosphate

A generic version of PRIMAQUINE PHOSPHATE was approved as primaquine phosphate by BAYSHORE PHARMS LLC on February 25th, 2014.

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Summary for PRIMAQUINE PHOSPHATE
Drug patent expirations by year for PRIMAQUINE PHOSPHATE
Recent Clinical Trials for PRIMAQUINE PHOSPHATE

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SponsorPhase
University of California, San FranciscoPhase 2/Phase 3
Pan American Health OrganizationPhase 2/Phase 3
Mahidol Oxford Tropical Medicine Research UnitPhase 4

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Pharmacology for PRIMAQUINE PHOSPHATE
Drug ClassAntimalarial
Medical Subject Heading (MeSH) Categories for PRIMAQUINE PHOSPHATE
Anatomical Therapeutic Chemical (ATC) Classes for PRIMAQUINE PHOSPHATE

US Patents and Regulatory Information for PRIMAQUINE PHOSPHATE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Alvogen PRIMAQUINE PHOSPHATE primaquine phosphate TABLET;ORAL 203924-001 Feb 3, 2014 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Bayshore Pharms Llc PRIMAQUINE PHOSPHATE primaquine phosphate TABLET;ORAL 204476-001 Feb 25, 2014 AB RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Novast Labs PRIMAQUINE PHOSPHATE primaquine phosphate TABLET;ORAL 206043-001 Jun 23, 2016 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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