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Last Updated: November 22, 2024

Details for New Drug Application (NDA): 019451


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NDA 019451 describes LOPRESSIDONE, which is a drug marketed by Novartis and is included in one NDA. Additional details are available on the LOPRESSIDONE profile page.

The generic ingredient in LOPRESSIDONE is chlorthalidone; metoprolol tartrate. There are twenty-one drug master file entries for this compound. Additional details are available on the chlorthalidone; metoprolol tartrate profile page.
Summary for 019451
Tradename:LOPRESSIDONE
Applicant:Novartis
Ingredient:chlorthalidone; metoprolol tartrate
Patents:0

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrength25MG;100MG
Approval Date:Dec 31, 1987TE:RLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrength25MG;200MG
Approval Date:Dec 31, 1987TE:RLD:No

Expired US Patents for NDA 019451

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Novartis LOPRESSIDONE chlorthalidone; metoprolol tartrate CAPSULE;ORAL 019451-001 Dec 31, 1987 ⤷  Sign Up ⤷  Sign Up
Novartis LOPRESSIDONE chlorthalidone; metoprolol tartrate CAPSULE;ORAL 019451-002 Dec 31, 1987 ⤷  Sign Up ⤷  Sign Up
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration

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