01 MOEHS IBERICA S. L. (1)
02 Cambrex Karlskoga AB (1)
03 Delta Synthetic Co. , Ltd. (1)
04 SWATI SPENTOSE PRIVATE LIMITED (1)
05 Spera Nexus Co., Ltd. (1)
06 Sumitomo Chemical Co., Ltd. (1)
01 Day stations lidocaine (production only) (1)
02 Japanese Pharmacopoeia lidocaine (1)
03 Lidocaine (4)
01 India (1)
02 Japan (2)
03 Spain (1)
04 Taiwan (1)
05 U.S.A (1)
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PharmaCompass offers a list of Lidocaine 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 Lidocaine manufacturer or Lidocaine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lidocaine manufacturer or Lidocaine supplier.
PharmaCompass also assists you with knowing the Lidocaine API Price utilized in the formulation of products. Lidocaine API Price is not always fixed or binding as the Lidocaine Price is obtained through a variety of data sources. The Lidocaine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LIDODERM manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LIDODERM, including repackagers and relabelers. The FDA regulates LIDODERM manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LIDODERM 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 LIDODERM manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LIDODERM supplier is an individual or a company that provides LIDODERM active pharmaceutical ingredient (API) or LIDODERM finished formulations upon request. The LIDODERM suppliers may include LIDODERM API manufacturers, exporters, distributors and traders.
click here to find a list of LIDODERM 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 LIDODERM Drug Master File in Japan (LIDODERM JDMF) empowers LIDODERM 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 LIDODERM JDMF during the approval evaluation for pharmaceutical products. At the time of LIDODERM 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 LIDODERM suppliers with JDMF on PharmaCompass.
We have 6 companies offering LIDODERM
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