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Looking for 18996-35-5 / Sodium Dihydrogen Citrate API manufacturers, exporters & distributors?

Sodium Dihydrogen Citrate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Sodium Dihydrogen Citrate

Synonyms

Citrofluyl, Monosodium dihydrogen citrate, Citric acid, monosodium salt, Citric acid monosodium salt, Sodium citrate monobasic, 68538up9se

Cas Number

18996-35-5

About Sodium Dihydrogen Citrate

Sodium salts of citric acid that are used as buffers and food preservatives. They are used medically as anticoagulants in stored blood, and for urine alkalization in the prevention of KIDNEY STONES.

Sodium Dihydrogen Citrate Manufacturers

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

Sodium Dihydrogen Citrate Suppliers

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

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

Sodium Dihydrogen Citrate GMP

Sodium Dihydrogen Citrate 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 Sodium Dihydrogen Citrate 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 Sodium Dihydrogen Citrate GMP manufacturer or Sodium Dihydrogen Citrate GMP API supplier for your needs.

Sodium Dihydrogen Citrate CoA

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

Sodium Dihydrogen Citrate CoA mostly includes findings from lab analyses of a specific batch. For each Sodium Dihydrogen Citrate 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.

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