DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
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01 1Dr. Reddy's Laboratories Ltd.
02 1Acebright (India) Pharma Private Limited
03 1Hetero Labs Limited
04 1SciAnda (Changshu) Pharmaceuticals, Ltd.
05 1Shandong Anxin Pharmaceutical Co. , Ltd.
06 1Shilpa Pharma Lifesciences Limited
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01 6Capecitabine
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01 2China
02 4India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 304MF10153
Registrant's Address : 8-2-337, Road No. 3, Banjara Hills, Hyderabad 500 034, TELANGANA, INDIA
Initial Date of Registration : 2022-12-07
Latest Date of Registration : 2022-12-07
Registration Number : 231MF10064
Registrant's Address : No. 77D & 116/117, KIADB Industrial Area, Jigani, Bangalore-560 105, Karnataka, INDIA
Initial Date of Registration : 2019-03-05
Latest Date of Registration : 2019-03-05
Registration Number : 228MF10215
Registrant's Address : 7-2-A2,Hetero Corporate,Industrial Estates Sanath Nagar,Hyderabad-500 018 Telangana I...
Initial Date of Registration : 2016-11-09
Latest Date of Registration : 2016-11-09
Registration Number : 304MF10148
Registrant's Address : No. 10678 Wenliang Road, Dongjia Town, Licheng District, Jinan, Shandong Province, P....
Initial Date of Registration : 2022-11-16
Latest Date of Registration : 2024-11-27
Registration Number : 229MF10104
Registrant's Address : No. 16, DongZhou Road Economic Development Zone Changshu, Jiangsu, China 215513
Initial Date of Registration : 2017-06-08
Latest Date of Registration : 2017-06-08
Registration Number : 229MF10131
Registrant's Address : Shilpa House, #12-6-214/A1, Hyderabad Road, Raichur-584 135, Karnataka, India
Initial Date of Registration : 2017-07-19
Latest Date of Registration : 2017-07-19
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PharmaCompass offers a list of Capecitabine 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 Capecitabine manufacturer or Capecitabine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Capecitabine manufacturer or Capecitabine supplier.
PharmaCompass also assists you with knowing the Capecitabine API Price utilized in the formulation of products. Capecitabine API Price is not always fixed or binding as the Capecitabine Price is obtained through a variety of data sources. The Capecitabine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ecansya manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ecansya, including repackagers and relabelers. The FDA regulates Ecansya manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ecansya 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 Ecansya manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ecansya supplier is an individual or a company that provides Ecansya active pharmaceutical ingredient (API) or Ecansya finished formulations upon request. The Ecansya suppliers may include Ecansya API manufacturers, exporters, distributors and traders.
click here to find a list of Ecansya 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 Ecansya Drug Master File in Japan (Ecansya JDMF) empowers Ecansya 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 Ecansya JDMF during the approval evaluation for pharmaceutical products. At the time of Ecansya 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 Ecansya suppliers with JDMF on PharmaCompass.
We have 6 companies offering Ecansya
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