Granules India has received USFDA’s approval for Methylergonovine 0.2 mg tablets. The abbreviated new drug applications (ANDA) was filed by Granules Pharmaceuticals Inc., a wholly...
Granules India hasΒ received Establishment Inspection Report (EIR), from the US health regulator for facility in Telangana. The US Food and Drug Administration inspected Jeedimetla facility...
Granules India has received EIR from US Food and Drug Administration (USFDA), for Chantilly unit. USFDA has issued establishment inspection report (EIR) for Granules Pharmaceuticals,...
Granules India, has received Establishment Inspection Report(EIR), for the OmniChem facility at Vizag, Andhra Pradesh, from the US health regulator. In a BSE filing it...
Granules India‘s board has provided its approval to the proposal to increase the foreign investment limit in the company to 49 percent. Granules India has...