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Last Updated: March 28, 2024

SORBITRATE Drug Patent Profile


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Which patents cover Sorbitrate, and what generic alternatives are available?

Sorbitrate is a drug marketed by Astrazeneca and is included in six NDAs.

The generic ingredient in SORBITRATE is isosorbide dinitrate. There are thirty-seven drug master file entries for this compound. Twenty-one suppliers are listed for this compound. Additional details are available on the isosorbide dinitrate profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Sorbitrate

A generic version of SORBITRATE was approved as isosorbide dinitrate by PAR PHARM on March 12th, 1987.

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Drug patent expirations by year for SORBITRATE
Recent Clinical Trials for SORBITRATE

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SponsorPhase
National Institute of PerinatologyPhase 4
National Council of Science and Technology, MexicoPhase 4

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US Patents and Regulatory Information for SORBITRATE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Astrazeneca SORBITRATE isosorbide dinitrate TABLET, CHEWABLE;ORAL 016776-002 Apr 1, 1996 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Astrazeneca SORBITRATE isosorbide dinitrate TABLET;ORAL 088125-001 Aug 21, 1990 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Astrazeneca SORBITRATE isosorbide dinitrate TABLET;ORAL 016192-002 Apr 1, 1996 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Astrazeneca SORBITRATE isosorbide dinitrate TABLET;SUBLINGUAL 016191-002 Apr 1, 1996 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Astrazeneca SORBITRATE isosorbide dinitrate TABLET, CHEWABLE;ORAL 016776-003 Apr 1, 1996 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Astrazeneca SORBITRATE isosorbide dinitrate TABLET;ORAL 016192-001 Apr 1, 1996 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Astrazeneca SORBITRATE isosorbide dinitrate TABLET;ORAL 088124-001 Aug 21, 1990 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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