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Hydrocortisone succinate

Registration Number : 219MF10308

Registrant's Address : 2-6-2 Otemachi, Chiyoda-ku, Tokyo

Initial Date of Registration : 2007-10-05

Latest Date of Registration : 2007-10-05

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Looking for 125-04-2 / Hydrocortisone Sodium Succinate API manufacturers, exporters & distributors?

Hydrocortisone Sodium Succinate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Hydrocortisone Sodium Succinate

Synonyms

125-04-2, A-hydrocort, Hydrocortisone 21-hemisuccinate sodium salt, Cortop, Solu-cortef, Arcocort

Cas Number

125-04-2

Unique Ingredient Identifier (UNII)

50LQB69S1Z

About Hydrocortisone Sodium Succinate

Hydrocortisone Sodium Succinate is the sodium salt of hydrocortisone succinate with glucocorticoid property. Hydrocortisone sodium succinate is chemically similar to the endogenous hormone that stimulates anti-inflammatory and immunosuppressive activities, in addition to exhibiting minor mineralocorticoid effects. This agent binds to intracellular glucocorticoid receptors and is translocated into the nucleus, where it initiates the transcription of glucocorticoid-responsive genes, such as various cytokines and lipocortins. Lipocortins inhibit phospholipase A2, thereby blocking the release of arachidonic acid from membrane phospholipids and preventing the synthesis of prostaglandins and leukotrienes, both potent mediators of inflammation.

Nositrol Manufacturers

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

Nositrol Suppliers

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

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

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

Nositrol Manufacturers | Traders | Suppliers

Nositrol Manufacturers, Traders, Suppliers 1
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We have 1 companies offering Nositrol

Get in contact with the supplier of your choice:

  1. Mutual Corporation
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.