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DOSAGE - TABLET;ORAL - 500MG
USFDA APPLICATION NUMBER - 20572
DOSAGE - POWDER;ORAL - 3GM/TEASPOONFUL
USFDA APPLICATION NUMBER - 20573
Related Excipient Companies
SPI Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Faran Shimi Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Healthcare
Gangwal Healthcare is powered by innovation, driving health, wellness & healing.
Dosage Form : Tablet
Grade : Oral
Application : Fillers, Diluents & Binders
Excipient Details : Microlose (Lactose Monohydrate & Microcrystalline Cellulose) is used as a diluent in oral dosage forms such as tablets.
Pharmacopoeia Ref : DMF, EXCiPAT, KOSHER, HALAL, W...
Technical Specs : Lactose Monohydrate – 40%, Microcrystalline cellulose – 60%
Ingredient(s) : Lactose Monohydrate
Gangwal Healthcare is powered by innovation, driving health, wellness & healing.
Dosage Form : Capsule
Grade : Oral
Application : Fillers, Diluents & Binders
Excipient Details : ProBlend (SMCC) is a co-processed excipient consists of microcrystalline cellulose & colloidal silicon dioxide, used as a diluent & binder in OSDs.
Pharmacopoeia Ref : USP-NF, DMF, EXCiPAT, KOSHER, ...
Technical Specs : NA
Ingredient(s) : Silicified Microcrystalline Cellulose
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Anhui Sunhere Pharmaceutical Excipients Co.,Ltd
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PharmaCompass offers a list of Sodium Phenylbutyrate 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 Phenylbutyrate manufacturer or Sodium Phenylbutyrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Phenylbutyrate manufacturer or Sodium Phenylbutyrate supplier.
PharmaCompass also assists you with knowing the Sodium Phenylbutyrate API Price utilized in the formulation of products. Sodium Phenylbutyrate API Price is not always fixed or binding as the Sodium Phenylbutyrate Price is obtained through a variety of data sources. The Sodium Phenylbutyrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A S4125,1716-12-7 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of S4125,1716-12-7, including repackagers and relabelers. The FDA regulates S4125,1716-12-7 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. S4125,1716-12-7 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 S4125,1716-12-7 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A S4125,1716-12-7 supplier is an individual or a company that provides S4125,1716-12-7 active pharmaceutical ingredient (API) or S4125,1716-12-7 finished formulations upon request. The S4125,1716-12-7 suppliers may include S4125,1716-12-7 API manufacturers, exporters, distributors and traders.
click here to find a list of S4125,1716-12-7 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A S4125,1716-12-7 DMF (Drug Master File) is a document detailing the whole manufacturing process of S4125,1716-12-7 active pharmaceutical ingredient (API) in detail. Different forms of S4125,1716-12-7 DMFs exist exist since differing nations have different regulations, such as S4125,1716-12-7 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A S4125,1716-12-7 DMF submitted to regulatory agencies in the US is known as a USDMF. S4125,1716-12-7 USDMF includes data on S4125,1716-12-7's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The S4125,1716-12-7 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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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 S4125,1716-12-7 Drug Master File in Japan (S4125,1716-12-7 JDMF) empowers S4125,1716-12-7 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 S4125,1716-12-7 JDMF during the approval evaluation for pharmaceutical products. At the time of S4125,1716-12-7 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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A S4125,1716-12-7 CEP of the European Pharmacopoeia monograph is often referred to as a S4125,1716-12-7 Certificate of Suitability (COS). The purpose of a S4125,1716-12-7 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of S4125,1716-12-7 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of S4125,1716-12-7 to their clients by showing that a S4125,1716-12-7 CEP has been issued for it. The manufacturer submits a S4125,1716-12-7 CEP (COS) as part of the market authorization procedure, and it takes on the role of a S4125,1716-12-7 CEP holder for the record. Additionally, the data presented in the S4125,1716-12-7 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the S4125,1716-12-7 DMF.
A S4125,1716-12-7 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. S4125,1716-12-7 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 S4125,1716-12-7 suppliers with CEP (COS) on PharmaCompass.
A S4125,1716-12-7 written confirmation (S4125,1716-12-7 WC) is an official document issued by a regulatory agency to a S4125,1716-12-7 manufacturer, verifying that the manufacturing facility of a S4125,1716-12-7 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting S4125,1716-12-7 APIs or S4125,1716-12-7 finished pharmaceutical products to another nation, regulatory agencies frequently require a S4125,1716-12-7 WC (written confirmation) as part of the regulatory process.
click here to find a list of S4125,1716-12-7 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 S4125,1716-12-7 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for S4125,1716-12-7 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 S4125,1716-12-7 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 S4125,1716-12-7 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a S4125,1716-12-7 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of S4125,1716-12-7 suppliers with NDC on PharmaCompass.
S4125,1716-12-7 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 S4125,1716-12-7 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 S4125,1716-12-7 GMP manufacturer or S4125,1716-12-7 GMP API supplier for your needs.
A S4125,1716-12-7 CoA (Certificate of Analysis) is a formal document that attests to S4125,1716-12-7's compliance with S4125,1716-12-7 specifications and serves as a tool for batch-level quality control.
S4125,1716-12-7 CoA mostly includes findings from lab analyses of a specific batch. For each S4125,1716-12-7 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.
S4125,1716-12-7 may be tested according to a variety of international standards, such as European Pharmacopoeia (S4125,1716-12-7 EP), S4125,1716-12-7 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (S4125,1716-12-7 USP).
