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Pharmacia & Upjohn Company Kalamazo...

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R0-CEP 2000-291 - Rev 00
Withdrawn by Holder
TSE
2001-10-24
2006-10-24
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01

Pharmacia & Upjohn Company Kalamazo...

Organic Process R&D
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Organic Process R&D
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Hydrocortisone-17-Butyrate

Certificate Number : R0-CEP 2000-291 - Rev 00

Status : Withdrawn by Holder

Issue Date : 2001-10-24

Type : TSE

Substance Number :

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Looking for 13609-67-1 / Hydrocortisone Butyrate API manufacturers, exporters & distributors?

Hydrocortisone Butyrate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Hydrocortisone Butyrate

Synonyms

Hydrocortisone 17-butyrate, Cortisol 17-butyrate, Hydrocortisone-17-butyrate, 13609-67-1, Locoid, Hydrocortisone-17alpha-butyrate

Cas Number

13609-67-1

Unique Ingredient Identifier (UNII)

05RMF7YPWN

About Hydrocortisone Butyrate

Hydrocortisone Butyrate is the butyrate salt form of hydrocortisone, a synthetic glucocorticoid receptor agonist with antiinflammatory, antipruritic and vasoconstrictive effects. Binding and activation of the glucocorticoid receptor results in the activation of lipocortin that in turn inhibits cytosolic phospholipase A2. Lack of phospholipase A2 prevents the release of arachidonic acid, precursor for inflammatory mediator prostaglandins and leukotrienes, from the cell membrane. Secondly, mitogen-activated protein kinase (MAPK) phosphatase 1 is induced, thereby leading to dephosphorylation and inactivation of Jun N-terminal kinase directly inhibiting c-Jun mediated transcription. Finally, transcriptional activity of nuclear factor (NF)-kappa-B is blocked, thereby inhibits the transcription of cyclooxygenase 2, which is essential for prostaglandin production.

Hydrocortisone Probutate Manufacturers

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

Hydrocortisone Probutate Suppliers

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

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

Hydrocortisone Probutate CEP

A Hydrocortisone Probutate CEP of the European Pharmacopoeia monograph is often referred to as a Hydrocortisone Probutate Certificate of Suitability (COS). The purpose of a Hydrocortisone Probutate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Hydrocortisone Probutate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Hydrocortisone Probutate to their clients by showing that a Hydrocortisone Probutate CEP has been issued for it. The manufacturer submits a Hydrocortisone Probutate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Hydrocortisone Probutate CEP holder for the record. Additionally, the data presented in the Hydrocortisone Probutate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Hydrocortisone Probutate DMF.

A Hydrocortisone Probutate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Hydrocortisone Probutate CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

click here to find a list of Hydrocortisone Probutate suppliers with CEP (COS) on PharmaCompass.

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.