01 2Eli Lilly and Company
02 3Lilly del Caribe, Inc.
01 1Insulin lispro (genetical recombination)
02 4Insulin lispro (recombinant)
01 5U.S.A
Registration Number : 303MF10175
Registrant's Address : 65th Infantry Road, Km. 12.6, Carolina, Puerto Rico 00985
Initial Date of Registration : 2021-12-09
Latest Date of Registration : 2026-01-08
Registration Number : 229MF10064
Registrant's Address : 65th Infantry Road, Km. 12.6, Carolina, Puerto Rico 00985
Initial Date of Registration : 2017-03-13
Latest Date of Registration : 2017-12-25
Registration Number : 226MF10225
Registrant's Address : Lilly Corporate Center, Indianapolis, Indiana 46285, USA
Initial Date of Registration : 2014-12-08
Latest Date of Registration : 2017-12-25
Registration Number : 219MF10053
Registrant's Address : 65th Infantry Road, Km. 12.6, Carolina, Puerto Rico 00985
Initial Date of Registration : 2007-03-05
Latest Date of Registration : 2017-12-25
Registration Number : 217MF10534
Registrant's Address : Lilly Corporate Center, Indianapolis, Indiana 46285, USA
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2017-12-25
41
PharmaCompass offers a list of Insulin Lispro 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 Insulin Lispro manufacturer or Insulin Lispro supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Insulin Lispro manufacturer or Insulin Lispro supplier.
PharmaCompass also assists you with knowing the Insulin Lispro API Price utilized in the formulation of products. Insulin Lispro API Price is not always fixed or binding as the Insulin Lispro Price is obtained through a variety of data sources. The Insulin Lispro Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Liprolog manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Liprolog, including repackagers and relabelers. The FDA regulates Liprolog manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Liprolog 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 Liprolog manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Liprolog supplier is an individual or a company that provides Liprolog active pharmaceutical ingredient (API) or Liprolog finished formulations upon request. The Liprolog suppliers may include Liprolog API manufacturers, exporters, distributors and traders.
click here to find a list of Liprolog 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 Liprolog Drug Master File in Japan (Liprolog JDMF) empowers Liprolog 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 Liprolog JDMF during the approval evaluation for pharmaceutical products. At the time of Liprolog 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 Liprolog suppliers with JDMF on PharmaCompass.
