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01 2Farmabios S. p. A.
02 2Curia Spain S. A. U.
03 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
01 1Day stations triamcinolone acetonide
02 1Day stations triamcinolone acetonide sterile
03 1Triamcinolone Acetonide
04 1Triamcinolone acetonide (Teva)
05 1Triamcinolone acetonide sterile
01 2Germany
02 1Italy
03 2U.S.A
Registration Number : 305MF10085
Registrant's Address : Via Pavia, 1-27027 Gropello Cairoli, Pavia, Italy
Initial Date of Registration : 2023-07-19
Latest Date of Registration : 2023-07-19
Triamcinolone acetonide Sterile
Registration Number : 223MF10049
Registrant's Address : Via Pavia, 1-27027 Gropello Cairoli, Pavia, Italy
Initial Date of Registration : 2011-04-12
Latest Date of Registration : 2020-01-31
Japanese Pharmacopoeia Triamcinolone Acetonide
Registration Number : 220MF10216
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2008-10-17
Latest Date of Registration : 2008-10-17
JP Triamcinolone Acetonide Sterile
Registration Number : 221MF10001
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2009-01-13
Latest Date of Registration : 2019-12-03
Triamcinolone acetonide (Teva)
Registration Number : 218MF10531
Registrant's Address : Piazzale Luigi Cadorna, 4 - 20123 MILANO, Italy
Initial Date of Registration : 2006-06-01
Latest Date of Registration : 2021-12-22
A Triamcinolone Acetonide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triamcinolone Acetonide, including repackagers and relabelers. The FDA regulates Triamcinolone Acetonide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triamcinolone Acetonide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Triamcinolone Acetonide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Triamcinolone Acetonide supplier is an individual or a company that provides Triamcinolone Acetonide active pharmaceutical ingredient (API) or Triamcinolone Acetonide finished formulations upon request. The Triamcinolone Acetonide suppliers may include Triamcinolone Acetonide API manufacturers, exporters, distributors and traders.
click here to find a list of Triamcinolone Acetonide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 Triamcinolone Acetonide Drug Master File in Japan (Triamcinolone Acetonide JDMF) empowers Triamcinolone Acetonide 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 Triamcinolone Acetonide JDMF during the approval evaluation for pharmaceutical products. At the time of Triamcinolone Acetonide JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Triamcinolone Acetonide suppliers with JDMF on PharmaCompass.
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