loader
Please Wait
Applying Filters...

Athena Athena

X

List of Drug Master Files (DMF) for 23977 Active Pharmaceutical Ingredient (API) submitted to the U.S. FDA. Original Data : FDA Website

Client Virtual Booth
Menu
Filters Filter
Cross PopUp
FILTER :

filter

01 Aarti Pharmalabs (1)

filter

01 MOMETASONE FUROATE MONOHYDRATE (1)

filter

01 India (1)

filter

01 Active (1)

filter

01 Blank (1)

Looking for Drug Master Files (DMF) for 23977 of Aarti Pharmalabs Ltd

Looking for Drug Master Files (DMF) for 23977 of Aarti Pharmalabs Ltd 1

20

Aarti Pharmalabs Ltd, based in India, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

They are recognized for Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.

One of their notable products is MOMETASONE FUROATE MONOHYDRATE, with a corresponding US DMF Number 23977.

Remarkably, this DMF maintains an Active status since its submission on July 14, 2010, highlighting commitment to regulatory compliance.

Post Enquiry
POST ENQUIRY