X
API Suppliers
US DMFs Filed
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
0
Other Suppliers
0
0
USA (Orange Book)
Europe
Canada
Australia
0
South Africa
0
Uploaded Dossiers
U.S. Medicaid
Annual Reports
0
45
PharmaCompass offers a list of Procarbazine 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 Procarbazine Hydrochloride manufacturer or Procarbazine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Procarbazine Hydrochloride manufacturer or Procarbazine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Procarbazine Hydrochloride API Price utilized in the formulation of products. Procarbazine Hydrochloride API Price is not always fixed or binding as the Procarbazine Hydrochloride Price is obtained through a variety of data sources. The Procarbazine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Indicarb manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Indicarb, including repackagers and relabelers. The FDA regulates Indicarb manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Indicarb 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 Indicarb manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Indicarb supplier is an individual or a company that provides Indicarb active pharmaceutical ingredient (API) or Indicarb finished formulations upon request. The Indicarb suppliers may include Indicarb API manufacturers, exporters, distributors and traders.
click here to find a list of Indicarb suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Indicarb DMF (Drug Master File) is a document detailing the whole manufacturing process of Indicarb active pharmaceutical ingredient (API) in detail. Different forms of Indicarb DMFs exist exist since differing nations have different regulations, such as Indicarb USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Indicarb DMF submitted to regulatory agencies in the US is known as a USDMF. Indicarb USDMF includes data on Indicarb's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Indicarb USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Indicarb 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 Indicarb as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Indicarb 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 Indicarb 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 Indicarb and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Indicarb NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Indicarb suppliers with NDC on PharmaCompass.
Indicarb 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 Indicarb 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 Indicarb GMP manufacturer or Indicarb GMP API supplier for your needs.
A Indicarb CoA (Certificate of Analysis) is a formal document that attests to Indicarb's compliance with Indicarb specifications and serves as a tool for batch-level quality control.
Indicarb CoA mostly includes findings from lab analyses of a specific batch. For each Indicarb 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.
Indicarb may be tested according to a variety of international standards, such as European Pharmacopoeia (Indicarb EP), Indicarb JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Indicarb USP).
Market Place
