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Last Updated: March 29, 2024

Details for New Drug Application (NDA): 020625


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NDA 020625 describes ALLEGRA, which is a drug marketed by Chattem Sanofi and is included in five NDAs. Additional details are available on the ALLEGRA profile page.

The generic ingredient in ALLEGRA is fexofenadine hydrochloride; pseudoephedrine hydrochloride. There are twenty-three drug master file entries for this compound. Twenty-seven suppliers are listed for this compound. Additional details are available on the fexofenadine hydrochloride; pseudoephedrine hydrochloride profile page.
Summary for 020625
Tradename:ALLEGRA
Applicant:Chattem Sanofi
Ingredient:fexofenadine hydrochloride
Patents:0
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrength60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date:Jul 25, 1996TE:RLD:No

Expired US Patents for NDA 020625

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Chattem Sanofi ALLEGRA fexofenadine hydrochloride CAPSULE;ORAL 020625-001 Jul 25, 1996 ⤷  Try a Trial ⤷  Try a Trial
Chattem Sanofi ALLEGRA fexofenadine hydrochloride CAPSULE;ORAL 020625-001 Jul 25, 1996 ⤷  Try a Trial ⤷  Try a Trial
Chattem Sanofi ALLEGRA fexofenadine hydrochloride CAPSULE;ORAL 020625-001 Jul 25, 1996 ⤷  Try a Trial ⤷  Try a Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration

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