Drug agency AstraZeneca Pharma India on Sunday stated it has acquired import and market permission from the Indian drug regulator for Selumetinib capsules.
The corporate has acquired the import and market permission in Kind CT-20 from the Medicine Controller Basic of India for Selumetinib 10 mg & 25 mg capsules, AstraZeneca Pharma India stated in a regulatory submitting.
The receipt of this permission paves means for the launch of Selumetinib 10 mg & 25 mg capsules in India, topic to the receipt of associated statutory approvals and licenses, it added.
Selumetinib 10 mg & 25 mg capsules are indicated for therapy of pediatric sufferers 3 years of age and older with neurofibromatosis kind 1 and who’ve symptomatic, inoperable plexiform neurofibromas, it added.
(Solely the headline and film of this report might have been reworked by the Enterprise Commonplace employees; the remainder of the content material is auto-generated from a syndicated feed.)
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