Ajanta Pharma gets USFDA curtsy for migraine pain service drug

NEW DELHI: Ajanta Pharma has perceived final capitulation for a general chronicle of strident migraine pain use drug almotriptan malate tablets from a US health regulator.

The capitulation by a US Food and Drug Administration (USFDA) is for mixed strengths of 6.25mg and 12.5mg of a general chronicle of Janssen Pharmaceuticals’ Axert tablets, Ajanta Pharma pronounced in a BSE filing.

Ajanta Pharma USA Inc, a wholly-owned auxiliary of a company, is scheduled to launch a almotriptan malate tablets in a US shortly, it said.

Almotriptan tablets is a partial of an “ever flourishing portfolio” that a association has grown for a US market, a association added.

The USFDA has so distant postulated final approvals for 8 shortened new drug applications (ANDAs) and dual indeterminate approvals, it said, adding that an additional 16 ANDAs are underneath review.

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