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01 2Farmabios S. p. A.
02 2Curia Spain S. A. U.
03 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
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01 1Day stations triamcinolone acetonide
02 1Day stations triamcinolone acetonide sterile
03 1Triamcinolone Acetonide
04 1Triamcinolone acetonide (Teva)
05 1Triamcinolone acetonide sterile
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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 : 2025-01-09
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
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PharmaCompass offers a list of Triamcinolone Acetonide 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 Triamcinolone Acetonide manufacturer or Triamcinolone Acetonide supplier for your needs.
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PharmaCompass also assists you with knowing the Triamcinolone Acetonide API Price utilized in the formulation of products. Triamcinolone Acetonide API Price is not always fixed or binding as the Triamcinolone Acetonide Price is obtained through a variety of data sources. The Triamcinolone Acetonide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Asmacort [Common Misspelling of Azmacort] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Asmacort [Common Misspelling of Azmacort], including repackagers and relabelers. The FDA regulates Asmacort [Common Misspelling of Azmacort] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Asmacort [Common Misspelling of Azmacort] 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 Asmacort [Common Misspelling of Azmacort] manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Asmacort [Common Misspelling of Azmacort] supplier is an individual or a company that provides Asmacort [Common Misspelling of Azmacort] active pharmaceutical ingredient (API) or Asmacort [Common Misspelling of Azmacort] finished formulations upon request. The Asmacort [Common Misspelling of Azmacort] suppliers may include Asmacort [Common Misspelling of Azmacort] API manufacturers, exporters, distributors and traders.
click here to find a list of Asmacort [Common Misspelling of Azmacort] 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 Asmacort [Common Misspelling of Azmacort] Drug Master File in Japan (Asmacort [Common Misspelling of Azmacort] JDMF) empowers Asmacort [Common Misspelling of Azmacort] 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 Asmacort [Common Misspelling of Azmacort] JDMF during the approval evaluation for pharmaceutical products. At the time of Asmacort [Common Misspelling of Azmacort] 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 Asmacort [Common Misspelling of Azmacort] suppliers with JDMF on PharmaCompass.
We have 3 companies offering Asmacort [Common Misspelling of Azmacort]
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