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Last Updated: April 26, 2024

Details for New Drug Application (NDA): 018166


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NDA 018166 describes TRASICOR, which is a drug marketed by Novartis and is included in one NDA. Additional details are available on the TRASICOR profile page.

The generic ingredient in TRASICOR is oxprenolol hydrochloride. There is one drug master file entry for this compound. Additional details are available on the oxprenolol hydrochloride profile page.
Summary for 018166
Tradename:TRASICOR
Applicant:Novartis
Ingredient:oxprenolol hydrochloride
Patents:0
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrength20MG
Approval Date:Dec 28, 1983TE:RLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrength40MG
Approval Date:Dec 28, 1983TE:RLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrength80MG
Approval Date:Dec 28, 1983TE:RLD:No

Expired US Patents for NDA 018166

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Novartis TRASICOR oxprenolol hydrochloride CAPSULE;ORAL 018166-004 Dec 28, 1983 ⤷  Try a Trial ⤷  Try a Trial
Novartis TRASICOR oxprenolol hydrochloride CAPSULE;ORAL 018166-002 Dec 28, 1983 ⤷  Try a Trial ⤷  Try a Trial
Novartis TRASICOR oxprenolol hydrochloride CAPSULE;ORAL 018166-003 Dec 28, 1983 ⤷  Try a Trial ⤷  Try a Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration

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