Pharmabiz
 

Zydus’ Nesher gets ANDA approval for dextroamphetamine from US FDA

Our Bureau, MumbaiThursday, March 31, 2016, 15:20 Hrs  [IST]

Nesher Pharmaceuticals, a subsidiary of Zydus Pharmaceuticals USA has received its first ANDA approval from the US FDA to market dextroamphetamine IR tabs.  The drug falls in the CNS stimulant segment and is the first product to be developed by the R&D team at Nesher. The drug will be produced at the manufacturing facility based at St. Louis, Missouri, USA.

The estimated sales for dextroamphetamine IR tabs is US $40.6 million as per IMS Health.

Nesher has considerable expertise in niche therapies which have development or production barriers, such as controlled release medications or DEA-controlled substances, which otherwise cannot be imported.

 
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