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PharmaCompass offers a list of Lamotrigine 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 Lamotrigine manufacturer or Lamotrigine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lamotrigine manufacturer or Lamotrigine supplier.
PharmaCompass also assists you with knowing the Lamotrigine API Price utilized in the formulation of products. Lamotrigine API Price is not always fixed or binding as the Lamotrigine Price is obtained through a variety of data sources. The Lamotrigine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lamictal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lamictal, including repackagers and relabelers. The FDA regulates Lamictal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lamictal 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 Lamictal manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lamictal supplier is an individual or a company that provides Lamictal active pharmaceutical ingredient (API) or Lamictal finished formulations upon request. The Lamictal suppliers may include Lamictal API manufacturers, exporters, distributors and traders.
click here to find a list of Lamictal suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 Lamictal Drug Master File in Japan (Lamictal JDMF) empowers Lamictal 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 Lamictal JDMF during the approval evaluation for pharmaceutical products. At the time of Lamictal 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 Lamictal suppliers with JDMF on PharmaCompass.
We have 5 companies offering Lamictal
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