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API SUPPLIERS
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
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USDMF
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Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Italy
Brand Name : Sucralfin
Dosage Form : Sucralfate 1.000Mg 40 Combined Oral Use
Dosage Strength : 40 CPR 1 g
Packaging :
Approval Date :
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Regulatory Info :
Registration Country : Italy
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Italy
Brand Name : Sucralfin
Dosage Form : Sucralfate 2.000Mg 30 Joined' Oral Use
Dosage Strength : os grat 30 bust 2 g
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Italy
Brand Name : SUCRALFIN
Dosage Form : Sachets
Dosage Strength : 2g
Packaging : 30 UNITS 2000 MG - ORAL USE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Italy
Brand Name : SUCRALFIN
Dosage Form : Tablet
Dosage Strength : 1g
Packaging : 40 UNITS 1000 MG - ORAL USE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Sweden
Brand Name : Andapsin
Dosage Form : ORAL SUSPENSION IN SACHET
Dosage Strength : 1 G / 5 ML
Packaging :
Approval Date :
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Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Andapsin
Dosage Form : ORAL SUSPENSION
Dosage Strength : 200 MG / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
Brand Name : Andapsin
Dosage Form : TABLET
Dosage Strength : 1 G
Packaging :
Approval Date :
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Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Norway
Brand Name : Antepsin
Dosage Form : Antic-calc Tablet
Dosage Strength : 1 g
Packaging : Blister
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Brand Name : Antepsin
Dosage Form : Antic-calc Tablet
Dosage Strength : 1 g
Packaging : Blister
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Brand Name : Antepsin
Dosage Form : Potion, suspension
Dosage Strength : 200 mg/ml
Packaging : Bottle
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
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DOSAGE - TABLET;ORAL - 1GM
USFDA APPLICATION NUMBER - 18333
DOSAGE - SUSPENSION;ORAL - 1GM/10ML
USFDA APPLICATION NUMBER - 19183
Related Excipient Companies
EUROAPI
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Rochem International Inc
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Dosage Form : Tablet
Grade : Oral
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27 Jun 2023
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ABOUT THIS PAGE
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PharmaCompass offers a list of Sucralfate 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 Sucralfate manufacturer or Sucralfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sucralfate manufacturer or Sucralfate supplier.
PharmaCompass also assists you with knowing the Sucralfate API Price utilized in the formulation of products. Sucralfate API Price is not always fixed or binding as the Sucralfate Price is obtained through a variety of data sources. The Sucralfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sucralfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sucralfate, including repackagers and relabelers. The FDA regulates Sucralfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sucralfate 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 Sucralfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sucralfate supplier is an individual or a company that provides Sucralfate active pharmaceutical ingredient (API) or Sucralfate finished formulations upon request. The Sucralfate suppliers may include Sucralfate API manufacturers, exporters, distributors and traders.
click here to find a list of Sucralfate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sucralfate DMF (Drug Master File) is a document detailing the whole manufacturing process of Sucralfate active pharmaceutical ingredient (API) in detail. Different forms of Sucralfate DMFs exist exist since differing nations have different regulations, such as Sucralfate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sucralfate DMF submitted to regulatory agencies in the US is known as a USDMF. Sucralfate USDMF includes data on Sucralfate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sucralfate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sucralfate suppliers with USDMF on PharmaCompass.
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 Sucralfate Drug Master File in Japan (Sucralfate JDMF) empowers Sucralfate 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 Sucralfate JDMF during the approval evaluation for pharmaceutical products. At the time of Sucralfate 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 Sucralfate suppliers with JDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Sucralfate Drug Master File in Korea (Sucralfate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Sucralfate. The MFDS reviews the Sucralfate KDMF as part of the drug registration process and uses the information provided in the Sucralfate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Sucralfate 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 Sucralfate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Sucralfate suppliers with KDMF on PharmaCompass.
A Sucralfate CEP of the European Pharmacopoeia monograph is often referred to as a Sucralfate Certificate of Suitability (COS). The purpose of a Sucralfate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Sucralfate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Sucralfate to their clients by showing that a Sucralfate CEP has been issued for it. The manufacturer submits a Sucralfate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Sucralfate CEP holder for the record. Additionally, the data presented in the Sucralfate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Sucralfate DMF.
A Sucralfate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Sucralfate 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 Sucralfate suppliers with CEP (COS) on PharmaCompass.
A Sucralfate written confirmation (Sucralfate WC) is an official document issued by a regulatory agency to a Sucralfate manufacturer, verifying that the manufacturing facility of a Sucralfate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Sucralfate APIs or Sucralfate finished pharmaceutical products to another nation, regulatory agencies frequently require a Sucralfate WC (written confirmation) as part of the regulatory process.
click here to find a list of Sucralfate suppliers with Written Confirmation (WC) on PharmaCompass.
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 Sucralfate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sucralfate API and other APIs are published in this directory by the FDA.
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 Sucralfate 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.
The NDC directory also contains data on finished compounded human drug products that contain Sucralfate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sucralfate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sucralfate suppliers with NDC on PharmaCompass.
Sucralfate 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 Sucralfate 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 Sucralfate GMP manufacturer or Sucralfate GMP API supplier for your needs.
A Sucralfate CoA (Certificate of Analysis) is a formal document that attests to Sucralfate's compliance with Sucralfate specifications and serves as a tool for batch-level quality control.
Sucralfate CoA mostly includes findings from lab analyses of a specific batch. For each Sucralfate 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.
Sucralfate may be tested according to a variety of international standards, such as European Pharmacopoeia (Sucralfate EP), Sucralfate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sucralfate USP).
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