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List of Drug Master Files (JDMF) for SODIUM SULFATE ANHYDROUS Active Pharmaceutical Ingredient (API) submitted to the Review Authority in Japan (PMDA). Original Data : PMDA Database

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01 Tomita Pharmaceutical Co., Ltd. (1)

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01 Pharmaceutical dried sodium sulfate 60SH (1)

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01 Japan (1)

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228MF10107
85-1 Maruyama, Myojin, Seto-cho, Na...
2016-06-06
2016-06-06
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Looking for 7757-82-6 / Sodium Sulfate API manufacturers, exporters & distributors?

Sodium Sulfate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Sodium Sulfate

Synonyms

7757-82-6, Disodium sulfate, Sodium sulfate, anhydrous, Sodium sulfate anhydrous, Sodium sulphate, Salt cake

Cas Number

7757-82-6

Unique Ingredient Identifier (UNII)

36KCS0R750

About Sodium Sulfate

Sodium Sulfate Anhydrous is the anhydrous, sodium salt form of sulfuric acid. Sodium sulfate anhydrous disassociates in water to provide sodium ions and sulfate ions. Sodium ion is the principal cation of the extracellular fluid and plays a large part in the therapy of fluid and electrolyte disturbances. Sodium sulfate anhydrous is an electrolyte replenisher and is used in isosmotic solutions so that administration does not disturb normal electrolyte balance and does not lead to absorption or excretion of water and ions.

SODIUM SULFATE ANHYDROUS Manufacturers

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

SODIUM SULFATE ANHYDROUS Suppliers

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

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

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

SODIUM SULFATE ANHYDROUS Manufacturers | Traders | Suppliers

SODIUM SULFATE ANHYDROUS Manufacturers, Traders, Suppliers 1
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We have 1 companies offering SODIUM SULFATE ANHYDROUS

Get in contact with the supplier of your choice:

  1. Tomita Pharmaceutical Co., Ltd.
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.
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