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Atosiban SUN (atosiban)

Generic
Region
🇪🇺 EU
Active substance
atosiban
Company
Sun Pharmaceutical Industries Europe B.V.
Status
Authorised
Therapeutic area
Obstetric Labor, Premature
EU approval
Wed 31 Jul 2013
Designations
Generic
Application
EMEA/H/C/002329
ATC
G02CX01
Official record
www.ema.europa.eu

Indication

Atosiban is indicated to delay imminent pre-term birth in pregnant adult women with: regular uterine contractions of at least 30 seconds’ duration at a rate of ? 4 per 30 minutes; a cervical dilation of 1 to 3 cm (0-3 for nulliparas) and effacement of ? 50%; a gestational age from 24 until 33 completed weeks; a normal foetal heart rate.

Regulatory milestones

No milestones recorded in the last year.

Same substance in other markets

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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.