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Last Updated: November 21, 2024

NASACORT HFA Drug Patent Profile


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Which patents cover Nasacort Hfa, and when can generic versions of Nasacort Hfa launch?

Nasacort Hfa is a drug marketed by Sanofi Aventis Us and is included in one NDA.

The generic ingredient in NASACORT HFA is triamcinolone acetonide. There are fifty-one drug master file entries for this compound. Seventy-four suppliers are listed for this compound. Additional details are available on the triamcinolone acetonide profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Nasacort Hfa

A generic version of NASACORT HFA was approved as triamcinolone acetonide by TARO on October 1st, 1986.

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Summary for NASACORT HFA
Drug patent expirations by year for NASACORT HFA
Recent Clinical Trials for NASACORT HFA

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

SponsorPhase
Gail GauvreauN/A
Stanford UniversityPhase 4
SanofiPhase 4

See all NASACORT HFA clinical trials

US Patents and Regulatory Information for NASACORT HFA

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Sanofi Aventis Us NASACORT HFA triamcinolone acetonide SPRAY, METERED;NASAL 020784-001 Apr 7, 2004 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

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