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VMF
DRUG PRODUCT COMPOSITIONS0
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API SUPPLIERS
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USDMF
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API Imports and Exports
Drugs in Development
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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 - POWDER;INTRAMUSCULAR - 11.25MG
USFDA APPLICATION NUMBER - 20263
DOSAGE - POWDER;INTRAMUSCULAR - 15MG
USFDA APPLICATION NUMBER - 20263
DOSAGE - POWDER;INTRAMUSCULAR - 3.75MG,7.5MG ...DOSAGE - POWDER;INTRAMUSCULAR - 3.75MG,7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 20263
DOSAGE - POWDER;INTRAMUSCULAR - 30MG
USFDA APPLICATION NUMBER - 20263
DOSAGE - POWDER;INTRAMUSCULAR - 45MG
USFDA APPLICATION NUMBER - 20263
DOSAGE - POWDER;INTRAMUSCULAR - 7.5MG
USFDA APPLICATION NUMBER - 20263
DOSAGE - POWDER;INTRAMUSCULAR - 7.5MG,7.5MG *...DOSAGE - POWDER;INTRAMUSCULAR - 7.5MG,7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 20263
DOSAGE - INJECTABLE, TABLET;INTRAMUSCULAR, OR...DOSAGE - INJECTABLE, TABLET;INTRAMUSCULAR, ORAL - 11.25MG/VIAL,N/A;N/A,5MG
USFDA APPLICATION NUMBER - 203696
DOSAGE - INJECTABLE, TABLET;INTRAMUSCULAR, OR...DOSAGE - INJECTABLE, TABLET;INTRAMUSCULAR, ORAL - 3.75MG/VIAL,N/A;N/A,5MG
USFDA APPLICATION NUMBER - 203696
Related Excipient Companies
Nanjing Well Pharmaceutical
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ABOUT THIS PAGE
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PharmaCompass offers a list of Leuprolide Acetate 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 Leuprolide Acetate manufacturer or Leuprolide Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Leuprolide Acetate manufacturer or Leuprolide Acetate supplier.
PharmaCompass also assists you with knowing the Leuprolide Acetate API Price utilized in the formulation of products. Leuprolide Acetate API Price is not always fixed or binding as the Leuprolide Acetate Price is obtained through a variety of data sources. The Leuprolide Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LUPANETA PACK manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LUPANETA PACK, including repackagers and relabelers. The FDA regulates LUPANETA PACK manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LUPANETA PACK 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 LUPANETA PACK manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LUPANETA PACK supplier is an individual or a company that provides LUPANETA PACK active pharmaceutical ingredient (API) or LUPANETA PACK finished formulations upon request. The LUPANETA PACK suppliers may include LUPANETA PACK API manufacturers, exporters, distributors and traders.
click here to find a list of LUPANETA PACK suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A LUPANETA PACK DMF (Drug Master File) is a document detailing the whole manufacturing process of LUPANETA PACK active pharmaceutical ingredient (API) in detail. Different forms of LUPANETA PACK DMFs exist exist since differing nations have different regulations, such as LUPANETA PACK USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A LUPANETA PACK DMF submitted to regulatory agencies in the US is known as a USDMF. LUPANETA PACK USDMF includes data on LUPANETA PACK's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The LUPANETA PACK USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of LUPANETA PACK 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 LUPANETA PACK Drug Master File in Japan (LUPANETA PACK JDMF) empowers LUPANETA PACK 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 LUPANETA PACK JDMF during the approval evaluation for pharmaceutical products. At the time of LUPANETA PACK 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 LUPANETA PACK 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 LUPANETA PACK Drug Master File in Korea (LUPANETA PACK KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of LUPANETA PACK. The MFDS reviews the LUPANETA PACK KDMF as part of the drug registration process and uses the information provided in the LUPANETA PACK KDMF to evaluate the safety and efficacy of the drug.
After submitting a LUPANETA PACK 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 LUPANETA PACK API can apply through the Korea Drug Master File (KDMF).
click here to find a list of LUPANETA PACK suppliers with KDMF on PharmaCompass.
A LUPANETA PACK CEP of the European Pharmacopoeia monograph is often referred to as a LUPANETA PACK Certificate of Suitability (COS). The purpose of a LUPANETA PACK CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of LUPANETA PACK EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of LUPANETA PACK to their clients by showing that a LUPANETA PACK CEP has been issued for it. The manufacturer submits a LUPANETA PACK CEP (COS) as part of the market authorization procedure, and it takes on the role of a LUPANETA PACK CEP holder for the record. Additionally, the data presented in the LUPANETA PACK CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the LUPANETA PACK DMF.
A LUPANETA PACK CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. LUPANETA PACK 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 LUPANETA PACK suppliers with CEP (COS) on PharmaCompass.
A LUPANETA PACK written confirmation (LUPANETA PACK WC) is an official document issued by a regulatory agency to a LUPANETA PACK manufacturer, verifying that the manufacturing facility of a LUPANETA PACK active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting LUPANETA PACK APIs or LUPANETA PACK finished pharmaceutical products to another nation, regulatory agencies frequently require a LUPANETA PACK WC (written confirmation) as part of the regulatory process.
click here to find a list of LUPANETA PACK 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 LUPANETA PACK as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for LUPANETA PACK 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 LUPANETA PACK 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 LUPANETA PACK and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a LUPANETA PACK NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of LUPANETA PACK suppliers with NDC on PharmaCompass.
LUPANETA PACK 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 LUPANETA PACK 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 LUPANETA PACK GMP manufacturer or LUPANETA PACK GMP API supplier for your needs.
A LUPANETA PACK CoA (Certificate of Analysis) is a formal document that attests to LUPANETA PACK's compliance with LUPANETA PACK specifications and serves as a tool for batch-level quality control.
LUPANETA PACK CoA mostly includes findings from lab analyses of a specific batch. For each LUPANETA PACK 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.
LUPANETA PACK may be tested according to a variety of international standards, such as European Pharmacopoeia (LUPANETA PACK EP), LUPANETA PACK JP (Japanese Pharmacopeia) and the US Pharmacopoeia (LUPANETA PACK USP).
