01 1Tomita Pharmaceutical
01 1MAGNESIUM OXIDE USP LIGHT POWDER
01 1Japan
01 1Active
01 1Complete
GDUFA
DMF Review : Complete
Rev. Date : 2014-11-13
Pay. Date : 2014-11-05
DMF Number : 23205
Submission : 2009-10-20
Status : Active
Type : II
20
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 OXIDE USP LIGHT POWDER, with a corresponding US DMF Number 23205.
Remarkably, this DMF maintains an Active status since its submission on October 20, 2009, highlighting commitment to regulatory compliance.
Their GDUFA DMF Review was successfully complete, with a review date of November 13, 2014, and payment made on November 05, 2014, indicating their dedication to facilitating drug approvals, Categorized as Type II
