Synopsis
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VMF
DRUG PRODUCT COMPOSITIONS0
Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
API SUPPLIERS
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USDMF
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results] EU WC
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Canada
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]DRUG PRODUCT COMPOSITIONS
DOSAGE - CAPSULE;ORAL - EQ 150MG BASE
USFDA APPLICATION NUMBER - 50162
DOSAGE - CAPSULE;ORAL - EQ 300MG BASE
USFDA APPLICATION NUMBER - 50162
DOSAGE - CAPSULE;ORAL - EQ 75MG BASE
USFDA APPLICATION NUMBER - 50162
Related Excipient Companies
SPI Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Healthcare
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Nanjing Well Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Kirsch Pharma
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Dr. Paul Lohmann GmbH & Co. KGaA
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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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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Chemicals
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Ingredion Pharma Solutions
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Lonza Capsugel
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Seppic
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Shanghai Shenmei Pharmaceutical Technology Co., Ltd
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Sigachi Industries
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Silverline Chemicals
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Fillers, Diluents & Binders
Direct Compression
Granulation
Lubricants & Glidants
Empty Capsules
Coating Systems & Additives
Parenteral
Taste Masking
Topical
Thickeners and Stabilizers
Co-Processed Excipients
Film Formers & Plasticizers
Chewable & Orodispersible Aids
Emulsifying Agents
Solubilizers
Controlled & Modified Release
Disintegrants & Superdisintegrants
Surfactant & Foaming Agents
API Stability Enhancers
Digital Content
NEWS #PharmaBuzz
Global Sales Information
US Medicaid Prescriptions
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Market Place
REF. STANDARDS & IMPURITIES
ANALYTICAL
Analytical Methods
ABOUT THIS PAGE
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PharmaCompass offers a list of Clindamycin Hydrochloride 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 Clindamycin Hydrochloride manufacturer or Clindamycin Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clindamycin Hydrochloride manufacturer or Clindamycin Hydrochloride supplier.
PharmaCompass also assists you with knowing the Clindamycin Hydrochloride API Price utilized in the formulation of products. Clindamycin Hydrochloride API Price is not always fixed or binding as the Clindamycin Hydrochloride Price is obtained through a variety of data sources. The Clindamycin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dalacin (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dalacin (TN), including repackagers and relabelers. The FDA regulates Dalacin (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dalacin (TN) 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 Dalacin (TN) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dalacin (TN) supplier is an individual or a company that provides Dalacin (TN) active pharmaceutical ingredient (API) or Dalacin (TN) finished formulations upon request. The Dalacin (TN) suppliers may include Dalacin (TN) API manufacturers, exporters, distributors and traders.
click here to find a list of Dalacin (TN) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dalacin (TN) DMF (Drug Master File) is a document detailing the whole manufacturing process of Dalacin (TN) active pharmaceutical ingredient (API) in detail. Different forms of Dalacin (TN) DMFs exist exist since differing nations have different regulations, such as Dalacin (TN) USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dalacin (TN) DMF submitted to regulatory agencies in the US is known as a USDMF. Dalacin (TN) USDMF includes data on Dalacin (TN)'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dalacin (TN) USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dalacin (TN) 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 Dalacin (TN) Drug Master File in Japan (Dalacin (TN) JDMF) empowers Dalacin (TN) 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 Dalacin (TN) JDMF during the approval evaluation for pharmaceutical products. At the time of Dalacin (TN) 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 Dalacin (TN) 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 Dalacin (TN) Drug Master File in Korea (Dalacin (TN) KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Dalacin (TN). The MFDS reviews the Dalacin (TN) KDMF as part of the drug registration process and uses the information provided in the Dalacin (TN) KDMF to evaluate the safety and efficacy of the drug.
After submitting a Dalacin (TN) 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 Dalacin (TN) API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Dalacin (TN) suppliers with KDMF on PharmaCompass.
A Dalacin (TN) CEP of the European Pharmacopoeia monograph is often referred to as a Dalacin (TN) Certificate of Suitability (COS). The purpose of a Dalacin (TN) CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Dalacin (TN) EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Dalacin (TN) to their clients by showing that a Dalacin (TN) CEP has been issued for it. The manufacturer submits a Dalacin (TN) CEP (COS) as part of the market authorization procedure, and it takes on the role of a Dalacin (TN) CEP holder for the record. Additionally, the data presented in the Dalacin (TN) CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Dalacin (TN) DMF.
A Dalacin (TN) CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Dalacin (TN) 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 Dalacin (TN) suppliers with CEP (COS) on PharmaCompass.
A Dalacin (TN) written confirmation (Dalacin (TN) WC) is an official document issued by a regulatory agency to a Dalacin (TN) manufacturer, verifying that the manufacturing facility of a Dalacin (TN) active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Dalacin (TN) APIs or Dalacin (TN) finished pharmaceutical products to another nation, regulatory agencies frequently require a Dalacin (TN) WC (written confirmation) as part of the regulatory process.
click here to find a list of Dalacin (TN) 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 Dalacin (TN) as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Dalacin (TN) 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 Dalacin (TN) 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 Dalacin (TN) and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Dalacin (TN) NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Dalacin (TN) suppliers with NDC on PharmaCompass.
Dalacin (TN) 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 Dalacin (TN) 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 Dalacin (TN) GMP manufacturer or Dalacin (TN) GMP API supplier for your needs.
A Dalacin (TN) CoA (Certificate of Analysis) is a formal document that attests to Dalacin (TN)'s compliance with Dalacin (TN) specifications and serves as a tool for batch-level quality control.
Dalacin (TN) CoA mostly includes findings from lab analyses of a specific batch. For each Dalacin (TN) 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.
Dalacin (TN) may be tested according to a variety of international standards, such as European Pharmacopoeia (Dalacin (TN) EP), Dalacin (TN) JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dalacin (TN) USP).
