“The United States Food and Drug Administration (US-FDA) has approved its Abbreviated New Drug Applications (ANDA) for Methylergonovine 0.2 mg Tablets. The ANDA was filed by Granules Pharmaceuticals Inc., a wholly owned subsidiary of Granules India. The approved ANDA is the bioequivalent to the reference listed drug product (RLD), Methergine 0.2 MG,” the company said in a press release.
Methylergonovine is a semi—synthetic ergot alkaloid used for the prevention and control of postpartum haemorrhage, it added.
Till 09:39 am; a combined 2.6 million equity shares have already changed hands on the counter in first 30 minutes of trade on the BSE and NSE.
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