Axplora is your partner of choice for complex APIs.
01 2Farmabios S. p. A.
02 2Curia Spain S. A. U.
03 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
Axplora is your partner of choice for complex APIs.
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
Axplora is your partner of choice for complex APIs.
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
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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Triamcinolone Acetonide manufacturer or Triamcinolone Acetonide supplier.
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 Kenalog 40 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Kenalog 40, including repackagers and relabelers. The FDA regulates Kenalog 40 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Kenalog 40 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 Kenalog 40 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Kenalog 40 supplier is an individual or a company that provides Kenalog 40 active pharmaceutical ingredient (API) or Kenalog 40 finished formulations upon request. The Kenalog 40 suppliers may include Kenalog 40 API manufacturers, exporters, distributors and traders.
click here to find a list of Kenalog 40 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 Kenalog 40 Drug Master File in Japan (Kenalog 40 JDMF) empowers Kenalog 40 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 Kenalog 40 JDMF during the approval evaluation for pharmaceutical products. At the time of Kenalog 40 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 Kenalog 40 suppliers with JDMF on PharmaCompass.
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