Zydus Lifesciences Gets U.S. FDA Final Approval for Ascorbic Acid Injection ANDA

MT Newswires Live

08/21

Zydus Lifesciences (NSE:ZYDUSLIFE, BOM:532321) received final U.S. Food and Drug Administration approval for its Abbreviated New Drug Application (ANDA) for Ascorbic Acid Injection USP in two strengths.

The product is a generic equivalent of Ascor Injection and has been designated a Competitive Generic Therapy by the U.S. FDA, according to a Friday filing on Indian bourses. It is used for the short-term treatment of scurvy in patients aged 5 months and older who cannot take vitamin C orally.

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