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Zydus Cadila receives USFDA approval to market anti-viral drug

| | Mar 29, 2016, at 07:32 pm
Ahmedabad/Mumbai, Mar 29 (IBNS) Zydus Cadilla, a fully integrated, global healthcare provider, announced on Tuesday that it has received the final approval from the US FDA to market Acyclovir capsules USP, 200 mg.

The company has said that the drug, which falls under the anti-viral segment, will be produced at its formulation manufacturing facility in SEZ, Ahmedabad.

The group now has more than 100 approvals and has so far filed over 280 ANDAs since the commencement of the filing process in FY 2003-2004; an Abbreviated New Drug Application (ANDA) is an application for a US generic drug approval for an existing licensed medication or approved drug. 

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