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Regulatory Info : Generic
Registration Country : South Africa
Brand Name : THROFLAM-CO
Dosage Form : MOW
Dosage Strength : 22.5mg/15 ml
Packaging : 200X1mg/15 ml
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Throflam-Co
Dosage Form : SPO
Dosage Strength : 22.5mg/15ml
Packaging : 30X1mg/15ml
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Throflam
Dosage Form : MOW
Dosage Strength : 22.5mg/15ml
Packaging : 200X1mg/15ml
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Throflam
Dosage Form : SPO
Dosage Strength : 22.5mg/15ml
Packaging : 30X1mg/15ml
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
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ABOUT THIS PAGE
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PharmaCompass offers a list of Benzydamine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Benzydamine Hydrochloride manufacturer or Benzydamine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Benzydamine Hydrochloride manufacturer or Benzydamine Hydrochloride supplier.
A Benzydamine HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Benzydamine HCl, including repackagers and relabelers. The FDA regulates Benzydamine HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Benzydamine HCl 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 Benzydamine HCl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Benzydamine HCl supplier is an individual or a company that provides Benzydamine HCl active pharmaceutical ingredient (API) or Benzydamine HCl finished formulations upon request. The Benzydamine HCl suppliers may include Benzydamine HCl API manufacturers, exporters, distributors and traders.
click here to find a list of Benzydamine HCl suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information 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 Benzydamine HCl Drug Master File in Korea (Benzydamine HCl KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Benzydamine HCl. The MFDS reviews the Benzydamine HCl KDMF as part of the drug registration process and uses the information provided in the Benzydamine HCl KDMF to evaluate the safety and efficacy of the drug.
After submitting a Benzydamine HCl 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 Benzydamine HCl API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Benzydamine HCl suppliers with KDMF on PharmaCompass.
A Benzydamine HCl CEP of the European Pharmacopoeia monograph is often referred to as a Benzydamine HCl Certificate of Suitability (COS). The purpose of a Benzydamine HCl CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Benzydamine HCl EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Benzydamine HCl to their clients by showing that a Benzydamine HCl CEP has been issued for it. The manufacturer submits a Benzydamine HCl CEP (COS) as part of the market authorization procedure, and it takes on the role of a Benzydamine HCl CEP holder for the record. Additionally, the data presented in the Benzydamine HCl CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Benzydamine HCl DMF.
A Benzydamine HCl CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Benzydamine HCl 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 Benzydamine HCl suppliers with CEP (COS) on PharmaCompass.
A Benzydamine HCl written confirmation (Benzydamine HCl WC) is an official document issued by a regulatory agency to a Benzydamine HCl manufacturer, verifying that the manufacturing facility of a Benzydamine HCl active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Benzydamine HCl APIs or Benzydamine HCl finished pharmaceutical products to another nation, regulatory agencies frequently require a Benzydamine HCl WC (written confirmation) as part of the regulatory process.
click here to find a list of Benzydamine HCl suppliers with Written Confirmation (WC) on PharmaCompass.
Benzydamine HCl 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 Benzydamine HCl GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Benzydamine HCl GMP manufacturer or Benzydamine HCl GMP API supplier for your needs.
A Benzydamine HCl CoA (Certificate of Analysis) is a formal document that attests to Benzydamine HCl's compliance with Benzydamine HCl specifications and serves as a tool for batch-level quality control.
Benzydamine HCl CoA mostly includes findings from lab analyses of a specific batch. For each Benzydamine HCl 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.
Benzydamine HCl may be tested according to a variety of international standards, such as European Pharmacopoeia (Benzydamine HCl EP), Benzydamine HCl JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Benzydamine HCl USP).
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