Close
4

Athena Athena

X

Find Heparin Sodium manufacturers, exporters & distributors on PharmaCompass

PharmaCompass
Related ProductsRelated Products
API SUPPLIERS
API Suppliers

API Suppliers

US DMFs Filed

US DMFs Filed

CEP/COS Certifications

CEP/COS Certifications

JDMFs Filed

JDMFs Filed

Other Certificates

Other Certificates

Other Suppliers

Other Suppliers

API REF. PRICE (USD / KG)
INTERMEDIATES
DOSSIERS // FDF
USA (Orange Book)

USA (Orange Book)

Europe

Europe

Canada

Canada

Australia

Australia

South Africa

South Africa

Uploaded Dossiers

Uploaded Dossiers

GLOBAL SALES (USD Million)

U.S. Medicaid

Annual Reports

0

EXCIPIENTS
PATENTS & EXCLUSIVITIES

USFDA Orange Book Patents

0

USFDA Exclusivities

0

DIGITAL CONTENT

Blog #PharmaFlow

News

REF STANDARD

EDQM

USP

JP

Other Listed Suppliers

SERVICES

0

left grey arrow
right gray arrow
  • INJECTABLE;INJECTION - 1,000 UNITS/ML
  • INJECTABLE;INJECTION - 10,000 UNITS/ML
  • INJECTABLE;INJECTION - 20,000 UNITS/ML
  • INJECTABLE;INJECTION - 5,000 UNITS/ML
  • INJECTABLE;INJECTION - 1,000 UNITS/ML
  • INJECTABLE;INJECTION - 10,000 UNITS/ML
  • INJECTABLE;INJECTION - 5,000 UNITS/ML

Looking for / Heparin Sodium API manufacturers, exporters & distributors?

Heparin Sodium manufacturers, exporters & distributors 1

23

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

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

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

API | Excipient name

Heparin Sodium

Synonyms

(2s,3s,4r,5r,6r)-6-{[(2s,3s,4s,5r,6s)-6-{[(2r,3s,4s,5r)-2-carboxy-4,6-dihydroxy-5-(sulfooxy)oxan-3-yl]oxy}-2-hydroxy-4-(sulfomethyl)-5-(sulfooxy)oxan-3-yl]oxy}-3-{[(2r,3r,4r,5s,6r)-3-acetamido-4,5-dihydroxy-6-[(sulfooxy)methyl]oxan-2-yl]oxy}-4,5-dihydroxyoxane-2-carboxylic acid, Hepflush, Chembl526514, Gtpl4214, S01xa14, Bdbm50480251

About Heparin Sodium

A highly acidic mucopolysaccharide formed of equal parts of sulfated D-glucosamine and D-glucuronic acid with sulfaminic bridges. The molecular weight ranges from six to twenty thousand. Heparin occurs in and is obtained from liver, lung, mast cells, etc., of vertebrates. Its function is unknown, but it is used to prevent blood clotting in vivo and vitro, in the form of many different salts.

Bemiparin Manufacturers

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

Bemiparin Suppliers

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

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

Bemiparin USDMF

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

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

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

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

Bemiparin KDMF

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

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

After submitting a Bemiparin 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 Bemiparin API can apply through the Korea Drug Master File (KDMF).

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

Bemiparin CEP

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

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

Bemiparin WC

A Bemiparin written confirmation (Bemiparin WC) is an official document issued by a regulatory agency to a Bemiparin manufacturer, verifying that the manufacturing facility of a Bemiparin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Bemiparin APIs or Bemiparin finished pharmaceutical products to another nation, regulatory agencies frequently require a Bemiparin WC (written confirmation) as part of the regulatory process.

click here to find a list of Bemiparin suppliers with Written Confirmation (WC) on PharmaCompass.

Bemiparin 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 Bemiparin as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Bemiparin 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 Bemiparin 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 Bemiparin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Bemiparin NDC to their finished compounded human drug products, they may choose to do so.

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

Bemiparin GMP

Bemiparin 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 Bemiparin 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 Bemiparin GMP manufacturer or Bemiparin GMP API supplier for your needs.

Bemiparin CoA

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

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

Bemiparin may be tested according to a variety of international standards, such as European Pharmacopoeia (Bemiparin EP), Bemiparin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Bemiparin 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.
Ask Us for Pharmaceutical Supplier and Partner
Ask Us, Find A Supplier / Partner
No Commissions, No Strings Attached, Get Connected for FREE

What are you looking for?

How can we help you?

The request can't be empty

Please read our Privacy Policy carefully

You must agree to the privacy policy

The name can't be empty
The company can't be empty.
The email can't be empty Please enter a valid email.
The mobile can't be empty
Post Enquiry
POST ENQUIRY