Tomita Pharmaceutical Co Ltd, based in Japan, is a pharmaceutical company that stands out with its certifications from FDA.
One of their notable products is MAGNESIUM SULFATE HEPTAHYDRATE, with a corresponding US DMF Number 26301.
Remarkably, this DMF maintains an Active status since its submission on August 08, 2012, highlighting commitment to regulatory compliance.
Their GDUFA DMF Review was successfully complete, with a review date of May 21, 2014, and payment made on September 27, 2013, indicating their dedication to facilitating drug approvals, Categorized as Type II