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01 1Sanwa Chemical Co., Ltd.

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Vietnam Medi-Pharm Expo
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Adrenochrome monoaminoguanidine mesylate (for manufacturing only)

Registration Number : 218MF10557

Registrant's Address : 24-8 Tamura 9-chome, Hiratsuka City, Kanagawa Prefecture

Initial Date of Registration : 2006-06-02

Latest Date of Registration : 2010-03-23

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Looking for 50-01-1 / GUANIDINE HYDROCHLORIDE API API manufacturers, exporters & distributors?

GUANIDINE HYDROCHLORIDE API manufacturers, exporters & distributors 1

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PharmaCompass offers a list of GUANIDINE HYDROCHLORIDE API 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 GUANIDINE HYDROCHLORIDE API manufacturer or GUANIDINE HYDROCHLORIDE API supplier for your needs.

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

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

API | Excipient name

GUANIDINE HYDROCHLORIDE API

Synonyms

50-01-1, Guanidinium chloride, Guanidine hcl, Guanidine, monohydrochloride, Aminoformamidine hydrochloride, Guanidine;hydrochloride

Cas Number

50-01-1

Unique Ingredient Identifier (UNII)

3YQC9ZY4YB

About GUANIDINE HYDROCHLORIDE API

A strong organic base existing primarily as guanidium ions at physiological pH. It is found in the urine as a normal product of protein metabolism. It is also used in laboratory research as a protein denaturant. (From Martindale, the Extra Pharmacopoeia, 30th ed and Merck Index, 12th ed) It is also used in the treatment of myasthenia and as a fluorescent probe in HPLC.

Guanidine Phosphate Manufacturers

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

Guanidine Phosphate Suppliers

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

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

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

Guanidine Phosphate Manufacturers | Traders | Suppliers

Guanidine Phosphate Manufacturers, Traders, Suppliers 1
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We have 1 companies offering Guanidine Phosphate

Get in contact with the supplier of your choice:

  1. Sanwa Kagaku Kenkyusho
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.