← Drug database

Acomplia (rimonabant)

Region
🇪🇺 EU
Active substance
rimonabant
Company
sanofi-aventis
Status
Withdrawn
Therapeutic area
Obesity
EU approval
Mon 19 Jun 2006
Application
EMEA/H/C/000666
ATC
A08AX01
Official record
www.ema.europa.eu

Indication

As an adjunct to diet and exercise for the treatment of obese patients (BMI 30 kg/m2), or overweight patients (BMI 27 kg/m2) with associated risk factor(s), such as type 2 diabetes or dyslipidaemia (see section 5.1).

Regulatory milestones

No milestones recorded in the last year.

Same substance in other markets

Follow Acomplia

Get VigiEye Daily: approvals, opinions, safety actions and PDUFA dates every morning.

Information from official EMA, FDA, Federal Register and SEC records. Dates marked company-announced come from the company's own SEC filing; dates marked estimate are calculated, not official. Not investment or medical advice; always confirm on the source.