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FDA rejects Prochieve(Watson Pharma) for risk reduction in PreTerm Birth

Read time: 1 mins
Last updated:1st Mar 2012
Published:1st Mar 2012
Source: Pharmawand
Watson Pharma has received a complete response letter from the FDA for its New Drug Application for Prochieve ( progesterone vaginal gel 8%) for use in the reduction of risk of Preterm Birth in women with a singleton gestation and a short uterine cervical length in the mid-trimester of pregnancy.

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