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List of Drug Master Files (DMF) for 25052 Active Pharmaceutical Ingredient (API) submitted to the U.S. FDA. Original Data : FDA Website

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01 Dipharma (1)

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01 FESOTERODINE FUMARATE (1)

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01 Italy (1)

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01 Active (1)

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01 Complete (1)

URL Supplier Web Content
25052
Active
2011-06-16
Complete
2013-02-07
2012-11-09
II
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Looking for Drug Master Files (DMF) for 25052 of Dipharma Francis Srl

Looking for Drug Master Files (DMF) for 25052 of Dipharma Francis Srl 1

20

Dipharma Francis Srl, based in Italy, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

One of their notable products is FESOTERODINE FUMARATE, with a corresponding US DMF Number 25052.

Remarkably, this DMF maintains an Active status since its submission on June 16, 2011, highlighting commitment to regulatory compliance.

Their GDUFA DMF Review was successfully complete, with a review date of February 07, 2013, and payment made on November 09, 2012, indicating their dedication to facilitating drug approvals, Categorized as Type II

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