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Last Updated: March 19, 2024

Details for New Drug Application (NDA): 020632


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NDA 020632 describes MERIDIA, which is a drug marketed by Abbott and is included in one NDA. Additional details are available on the MERIDIA profile page.

The generic ingredient in MERIDIA is sibutramine hydrochloride. There are six drug master file entries for this compound. Additional details are available on the sibutramine hydrochloride profile page.
Summary for 020632
Tradename:MERIDIA
Applicant:Abbott
Ingredient:sibutramine hydrochloride
Patents:0
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrength5MG
Approval Date:Nov 22, 1997TE:RLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrength10MG
Approval Date:Nov 22, 1997TE:RLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrength15MG
Approval Date:Nov 22, 1997TE:RLD:No

Expired US Patents for NDA 020632

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Abbott MERIDIA sibutramine hydrochloride CAPSULE;ORAL 020632-003 Nov 22, 1997 ⤷  Try a Trial ⤷  Try a Trial
Abbott MERIDIA sibutramine hydrochloride CAPSULE;ORAL 020632-001 Nov 22, 1997 ⤷  Try a Trial ⤷  Try a Trial
Abbott MERIDIA sibutramine hydrochloride CAPSULE;ORAL 020632-002 Nov 22, 1997 ⤷  Try a Trial ⤷  Try a Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration

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