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PharmaCompass offers a list of Morphine Sulfate 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 Morphine Sulfate manufacturer or Morphine Sulfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Morphine Sulfate manufacturer or Morphine Sulfate supplier.
PharmaCompass also assists you with knowing the Morphine Sulfate API Price utilized in the formulation of products. Morphine Sulfate API Price is not always fixed or binding as the Morphine Sulfate Price is obtained through a variety of data sources. The Morphine Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Morphine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Morphine, including repackagers and relabelers. The FDA regulates Morphine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Morphine 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 Morphine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Morphine supplier is an individual or a company that provides Morphine active pharmaceutical ingredient (API) or Morphine finished formulations upon request. The Morphine suppliers may include Morphine API manufacturers, exporters, distributors and traders.
click here to find a list of Morphine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Morphine DMF (Drug Master File) is a document detailing the whole manufacturing process of Morphine active pharmaceutical ingredient (API) in detail. Different forms of Morphine DMFs exist exist since differing nations have different regulations, such as Morphine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Morphine DMF submitted to regulatory agencies in the US is known as a USDMF. Morphine USDMF includes data on Morphine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Morphine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Morphine suppliers with USDMF 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 Morphine Drug Master File in Korea (Morphine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Morphine. The MFDS reviews the Morphine KDMF as part of the drug registration process and uses the information provided in the Morphine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Morphine 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 Morphine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Morphine suppliers with KDMF on PharmaCompass.
A Morphine CEP of the European Pharmacopoeia monograph is often referred to as a Morphine Certificate of Suitability (COS). The purpose of a Morphine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Morphine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Morphine to their clients by showing that a Morphine CEP has been issued for it. The manufacturer submits a Morphine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Morphine CEP holder for the record. Additionally, the data presented in the Morphine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Morphine DMF.
A Morphine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Morphine 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 Morphine suppliers with CEP (COS) 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 Morphine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Morphine 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 Morphine 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 Morphine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Morphine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Morphine suppliers with NDC on PharmaCompass.
Morphine 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 Morphine 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 Morphine GMP manufacturer or Morphine GMP API supplier for your needs.
A Morphine CoA (Certificate of Analysis) is a formal document that attests to Morphine's compliance with Morphine specifications and serves as a tool for batch-level quality control.
Morphine CoA mostly includes findings from lab analyses of a specific batch. For each Morphine 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.
Morphine may be tested according to a variety of international standards, such as European Pharmacopoeia (Morphine EP), Morphine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Morphine USP).
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