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01 1Farmabios S. p. A.

02 1Sicor Societa (') Italiana Corticosteroidi S. r. l.

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PharmaCompass

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  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAxplora is your partner of choice for complex APIs.

Amcinonide

Registration Number : 305MF10048

Registrant's Address : Via Pavia, 1-27027 Gropello Cairoli, Pavia, Italy

Initial Date of Registration : 2023-04-12

Latest Date of Registration : 2023-04-12

Axplora CB

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Amcinonide "Teva"

Registration Number : 218MF10911

Registrant's Address : Piazzale Luigi Cadorna, 4 - 20123 MILANO, Italy

Initial Date of Registration : 2006-11-10

Latest Date of Registration : 2006-11-10

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Looking for 51022-69-6 / Amcinonide API manufacturers, exporters & distributors?

Amcinonide manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Amcinonide 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 Amcinonide manufacturer or Amcinonide supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Amcinonide manufacturer or Amcinonide supplier.

PharmaCompass also assists you with knowing the Amcinonide API Price utilized in the formulation of products. Amcinonide API Price is not always fixed or binding as the Amcinonide Price is obtained through a variety of data sources. The Amcinonide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Amcinonide

Synonyms

51022-69-6, Cyclocort, Amcinonidum, Cl-34699, Triamcinolonacetatcyclopentanonid, Cl 34699

Cas Number

51022-69-6

Unique Ingredient Identifier (UNII)

423W026MA9

About Amcinonide

Amcinonide is a synthetic glucocorticoid receptor agonist that mimics the metabolic, anti-inflammatory, and immunosuppressive activity of the natural glucocorticoids. Amcinonide interacts with specific corticosteroid receptors and was internalized, which leads to binding of DNA and modification of gene expression. This results in synthesis of anti-inflammatory mediators while inhibiting synthesis of inflammatory mediators. Consequently, an overall reduction in chronic inflammation and autoimmune reactions are achieved.

Mycoderm Manufacturers

A Mycoderm manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mycoderm, including repackagers and relabelers. The FDA regulates Mycoderm manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mycoderm 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 Mycoderm manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Mycoderm Suppliers

A Mycoderm supplier is an individual or a company that provides Mycoderm active pharmaceutical ingredient (API) or Mycoderm finished formulations upon request. The Mycoderm suppliers may include Mycoderm API manufacturers, exporters, distributors and traders.

click here to find a list of Mycoderm suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Mycoderm JDMF

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 Mycoderm Drug Master File in Japan (Mycoderm JDMF) empowers Mycoderm 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 Mycoderm JDMF during the approval evaluation for pharmaceutical products. At the time of Mycoderm 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 Mycoderm suppliers with JDMF on PharmaCompass.

Mycoderm Manufacturers | Traders | Suppliers

Mycoderm Manufacturers, Traders, Suppliers 1
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We have 2 companies offering Mycoderm

Get in contact with the supplier of your choice:

  1. Axplora
  2. Sicor Societa Italiana Corticosteroidi Srl
Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.