01 1MSD International GmbH (Singapore Branch)
02 3Sicor de Me(´)xico,S. A. de C. V.
03 3Sterling S. p. A.
04 1Sterling Srl
05 1Symbiotica Specialty Ingredients Sdn. Bhd.
01 1Mometasone Fluorate Monohydrate
02 2Mometasone Furoate
03 1Mometasone Furoate (Micronized)
04 1Mometasone Furoate Monohydrate
05 1Mometasone franc carboxylic acid ester "Teva"
06 1Mometasone furan carboxylate hydrate "Teva"
07 1Mometasone furan carboxylic acid ester hydrate
08 1Mometasone furoate
01 4Italy
02 1Malaysia
03 3Mexico
04 1Singapore
Registration Number : 218MF10890
Registrant's Address : 50 Tuas West Drive Singapore 638408
Initial Date of Registration : 2006-11-10
Latest Date of Registration : 2008-06-30
Registration Number : 220MF10138
Registrant's Address : Av. San Rafael No. 35 Parque Industrial Lerma, CP52000 Lerma, Edo. Me(´)xico. MEXICO
Initial Date of Registration : 2008-05-29
Latest Date of Registration : 2025-01-09
Mometasone furoate hydrate (Teva)
Registration Number : 228MF10160
Registrant's Address : Av. San Rafael No. 35 Parque Industrial Lerma, CP52000 Lerma, Edo. Me(´)xico. MEXICO
Initial Date of Registration : 2016-08-10
Latest Date of Registration : 2019-04-22
Mometasone furoate hydrate "Teva 2"
Registration Number : 304MF10036
Registrant's Address : Av. San Rafael No. 35 Parque Industrial Lerma, CP52000 Lerma, Edo. Me(´)xico. MEXICO
Initial Date of Registration : 2022-02-17
Latest Date of Registration : 2022-02-17
Mometasone Furoate (Micronized)
Registration Number : 220MF10120
Registrant's Address : Via Della Carboneria 30 Solomeo 06073 Corciano Perugia-Italy
Initial Date of Registration : 2008-04-28
Latest Date of Registration : 2022-10-26
Mometasone Furoate Monohydrate
Registration Number : 301MF10014
Registrant's Address : Via Della Carboneria 30 Solomeo 06073 Corciano Perugia-Italy
Initial Date of Registration : 2019-06-05
Latest Date of Registration : 2019-06-05
Mometasone Furoate Monohydrate
Registration Number : 228MF10133
Registrant's Address : Via Della Carboneria 30 Solomeo 06073 Corciano Perugia-Italy
Initial Date of Registration : 2016-07-25
Latest Date of Registration : 2016-07-25
Registration Number : 219MF10017
Registrant's Address : Via Della Carboneria 30 Solomeo 06073 Corciano Perugia-Italy
Initial Date of Registration : 2007-01-18
Latest Date of Registration : 2007-01-18
Registration Number : 304MF10102
Registrant's Address : No. 518, Jalan Waja 4, Taman Industry Waja, 09000 Kulim, Kedah Darul Aman, Malaysia
Initial Date of Registration : 2022-07-27
Latest Date of Registration : 2022-07-27
22
PharmaCompass offers a list of Mometasone Furoate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Mometasone Furoate manufacturer or Mometasone Furoate supplier for your needs.
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A Mometasone furoate [USAN:USP:JAN] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mometasone furoate [USAN:USP:JAN], including repackagers and relabelers. The FDA regulates Mometasone furoate [USAN:USP:JAN] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mometasone furoate [USAN:USP:JAN] API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Mometasone furoate [USAN:USP:JAN] supplier is an individual or a company that provides Mometasone furoate [USAN:USP:JAN] active pharmaceutical ingredient (API) or Mometasone furoate [USAN:USP:JAN] finished formulations upon request. The Mometasone furoate [USAN:USP:JAN] suppliers may include Mometasone furoate [USAN:USP:JAN] API manufacturers, exporters, distributors and traders.
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The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Mometasone furoate [USAN:USP:JAN] Drug Master File in Japan (Mometasone furoate [USAN:USP:JAN] JDMF) empowers Mometasone furoate [USAN:USP:JAN] API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Mometasone furoate [USAN:USP:JAN] JDMF during the approval evaluation for pharmaceutical products. At the time of Mometasone furoate [USAN:USP:JAN] JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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We have 4 companies offering Mometasone furoate [USAN:USP:JAN]
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