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API SUPPLIERS
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USDMF
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Neuland Laboratories- A dedicated 100% API provider.
About the Company : Neuland Laboratories, established in 1984 and headquartered in Hyderabad, is a publicly listed company offering solutions for pharmaceutical chemistry needs—from library compound...
Maithri Drugs: Dedicated to your API needs.
About the Company : Maithri Drugs Pvt. Ltd. is a global supplier of Active Pharmaceutical Ingredients (APIs), serving pharmaceutical companies in 60+ countries. Its API portfolio spans antivirals, ant...
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Olpha, a JSC AB City subsidiary, is a leading Baltic firm with 50 years of experience in medicines & chemical pharmaceuticals.
CAS Number : 1619-34-7
End Use API : Aceclidine Hydrochloride
About The Company : Olpha, a subsidiary of JSC AB City, is one of the largest companies in the Baltic states with 50 years of experience in producing medicines and chemical pharmac...
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PharmaCompass offers a list of Aceclidine 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 Aceclidine Hydrochloride manufacturer or Aceclidine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aceclidine Hydrochloride manufacturer or Aceclidine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Aceclidine Hydrochloride API Price utilized in the formulation of products. Aceclidine Hydrochloride API Price is not always fixed or binding as the Aceclidine Hydrochloride Price is obtained through a variety of data sources. The Aceclidine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aceclidine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aceclidine Hydrochloride, including repackagers and relabelers. The FDA regulates Aceclidine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aceclidine Hydrochloride 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 Aceclidine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aceclidine Hydrochloride supplier is an individual or a company that provides Aceclidine Hydrochloride active pharmaceutical ingredient (API) or Aceclidine Hydrochloride finished formulations upon request. The Aceclidine Hydrochloride suppliers may include Aceclidine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Aceclidine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Aceclidine Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Aceclidine Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Aceclidine Hydrochloride DMFs exist exist since differing nations have different regulations, such as Aceclidine Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Aceclidine Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Aceclidine Hydrochloride USDMF includes data on Aceclidine Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Aceclidine Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Aceclidine Hydrochloride suppliers with USDMF 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 Aceclidine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Aceclidine Hydrochloride 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 Aceclidine Hydrochloride 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 Aceclidine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Aceclidine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Aceclidine Hydrochloride suppliers with NDC on PharmaCompass.
Aceclidine Hydrochloride 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 Aceclidine Hydrochloride 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 Aceclidine Hydrochloride GMP manufacturer or Aceclidine Hydrochloride GMP API supplier for your needs.
A Aceclidine Hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Aceclidine Hydrochloride's compliance with Aceclidine Hydrochloride specifications and serves as a tool for batch-level quality control.
Aceclidine Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Aceclidine Hydrochloride 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.
Aceclidine Hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Aceclidine Hydrochloride EP), Aceclidine Hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Aceclidine Hydrochloride USP).
