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  • FOR SOLUTION;INTRAVENOUS - 80MG/VIAL;0.02MG/VIAL;0.001MG/VIAL;5MG/VIAL;0.01MG/VIAL;0.14MG/VIAL;17MG/VIAL;0.2MG/VIAL;1MG/VIAL;1.4MG/VIAL;EQ 1.2MG BASE/VIAL;0.7MG/VIAL;7MG/VIAL
  • SOLUTION;INTRAVENOUS - 2 IU/ML;40MG/ML;12MCG/ML;40 IU/ML;1MCG/ML;3MG/ML;120MCG/ML;8MG/ML;1.2MG/ML;0.72MG/ML;1.2MG/ML;660 IU/ML;0.03MG/ML
  • SOLUTION;INTRAVENOUS - 2 IU/ML;40MG/ML;12MCG/ML;40 IU/ML;1MCG/ML;3MG/ML;120MCG/ML;8MG/ML;1.2MG/ML;0.72MG/ML;1.2MG/ML;660 IU/ML;30MCG/ML
  • INJECTABLE;INTRAVENOUS - 200MG/VIAL;0.06MG/VIAL;0.005MG/VIAL;15MG/VIAL;0.005MG/VIAL;0.6MG/VIAL;40MG/VIAL;6MG/VIAL;3.6MG/VIAL;6MG/VIAL;1MG/VIAL;10MG/VIAL;0.15MG/VIAL
  • INJECTABLE;INJECTION - 20MG/ML;0.006MG/ML;0.05MCG/ML;1.5MG/ML;0.0005MG/ML;0.06MG/ML;4MG/ML;0.6MG/ML;0.36MG/ML;0.6MG/ML;0.1MG/ML;1MG/ML

Looking for 58-56-0 / Pyridoxine Hydrochloride API manufacturers, exporters & distributors?

Pyridoxine Hydrochloride manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Pyridoxine Hydrochloride

Synonyms

58-56-0, Pyridoxine hcl, Pyridoxol hydrochloride, Vitamin b6, Vitamin b6 hydrochloride, Pyridoxine chloride

Cas Number

58-56-0

Unique Ingredient Identifier (UNII)

68Y4CF58BV

About Pyridoxine Hydrochloride

The 4-methanol form of VITAMIN B 6 which is converted to PYRIDOXAL PHOSPHATE which is a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. Although pyridoxine and Vitamin B 6 are still frequently used as synonyms, especially by medical researchers, this practice is erroneous and sometimes misleading (EE Snell; Ann NY Acad Sci, vol 585 pg 1, 1990).

Benadon Manufacturers

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

Benadon Suppliers

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

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

Benadon USDMF

A Benadon DMF (Drug Master File) is a document detailing the whole manufacturing process of Benadon active pharmaceutical ingredient (API) in detail. Different forms of Benadon DMFs exist exist since differing nations have different regulations, such as Benadon USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Benadon DMF submitted to regulatory agencies in the US is known as a USDMF. Benadon USDMF includes data on Benadon's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Benadon USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Benadon suppliers with USDMF on PharmaCompass.

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

Benadon KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a Benadon Drug Master File in Korea (Benadon KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Benadon. The MFDS reviews the Benadon KDMF as part of the drug registration process and uses the information provided in the Benadon KDMF to evaluate the safety and efficacy of the drug.

After submitting a Benadon KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Benadon API can apply through the Korea Drug Master File (KDMF).

click here to find a list of Benadon suppliers with KDMF on PharmaCompass.

Benadon CEP

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

A Benadon CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Benadon 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 Benadon suppliers with CEP (COS) on PharmaCompass.

Benadon NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Benadon as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Benadon API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Benadon as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Benadon and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Benadon NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Benadon suppliers with NDC on PharmaCompass.

Benadon GMP

Benadon Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of Benadon GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Benadon GMP manufacturer or Benadon GMP API supplier for your needs.

Benadon CoA

A Benadon CoA (Certificate of Analysis) is a formal document that attests to Benadon's compliance with Benadon specifications and serves as a tool for batch-level quality control.

Benadon CoA mostly includes findings from lab analyses of a specific batch. For each Benadon CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

Benadon may be tested according to a variety of international standards, such as European Pharmacopoeia (Benadon EP), Benadon JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Benadon USP).

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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