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Looking for 1310-73-2 / Sodium Hydroxide API manufacturers, exporters & distributors?

Sodium Hydroxide manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Sodium Hydroxide

Synonyms

Caustic soda, 1310-73-2, Sodium hydrate, Aetznatron, Soda lye, White caustic

Cas Number

1310-73-2

Unique Ingredient Identifier (UNII)

55X04QC32I

About Sodium Hydroxide

A highly caustic substance that is used to neutralize acids and make sodium salts. (From Merck Index, 11th ed)

06208_RIEDEL Manufacturers

A 06208_RIEDEL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 06208_RIEDEL, including repackagers and relabelers. The FDA regulates 06208_RIEDEL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 06208_RIEDEL 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 06208_RIEDEL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

06208_RIEDEL Suppliers

A 06208_RIEDEL supplier is an individual or a company that provides 06208_RIEDEL active pharmaceutical ingredient (API) or 06208_RIEDEL finished formulations upon request. The 06208_RIEDEL suppliers may include 06208_RIEDEL API manufacturers, exporters, distributors and traders.

click here to find a list of 06208_RIEDEL suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

06208_RIEDEL USDMF

A 06208_RIEDEL DMF (Drug Master File) is a document detailing the whole manufacturing process of 06208_RIEDEL active pharmaceutical ingredient (API) in detail. Different forms of 06208_RIEDEL DMFs exist exist since differing nations have different regulations, such as 06208_RIEDEL USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 06208_RIEDEL DMF submitted to regulatory agencies in the US is known as a USDMF. 06208_RIEDEL USDMF includes data on 06208_RIEDEL's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 06208_RIEDEL USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 06208_RIEDEL suppliers with USDMF on PharmaCompass.

06208_RIEDEL 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 06208_RIEDEL Drug Master File in Japan (06208_RIEDEL JDMF) empowers 06208_RIEDEL 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 06208_RIEDEL JDMF during the approval evaluation for pharmaceutical products. At the time of 06208_RIEDEL 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 06208_RIEDEL suppliers with JDMF on PharmaCompass.

06208_RIEDEL GMP

06208_RIEDEL 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 06208_RIEDEL 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 06208_RIEDEL GMP manufacturer or 06208_RIEDEL GMP API supplier for your needs.

06208_RIEDEL CoA

A 06208_RIEDEL CoA (Certificate of Analysis) is a formal document that attests to 06208_RIEDEL's compliance with 06208_RIEDEL specifications and serves as a tool for batch-level quality control.

06208_RIEDEL CoA mostly includes findings from lab analyses of a specific batch. For each 06208_RIEDEL 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.

06208_RIEDEL may be tested according to a variety of international standards, such as European Pharmacopoeia (06208_RIEDEL EP), 06208_RIEDEL JP (Japanese Pharmacopeia) and the US Pharmacopoeia (06208_RIEDEL 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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