01 1Alives Life Sciences Limited
02 3FORMOSA LABORATORIES, INC.
03 1JUBILANT PHARMOVA LIMITED
01 1For linezolid oral
02 4Linezolid
01 2India
02 3Taiwan
Registration Number : 229MF10166
Registrant's Address : 4th Floor, OIA House, 470, Cardinal Gracious Road, Andheri East Mumbai 400099, Mahara...
Initial Date of Registration : 2017-08-22
Latest Date of Registration : 2018-05-21
Registration Number : 226MF10166
Registrant's Address : 36 Hoping Street, Louchu, Taoyuan 33842, Taiwan
Initial Date of Registration : 2014-09-01
Latest Date of Registration : 2014-11-17
Registration Number : 225MF10170
Registrant's Address : 36 Hoping Street, Louchu, Taoyuan 33842, Taiwan
Initial Date of Registration : 2013-08-28
Latest Date of Registration : 2014-11-17
Registration Number : 302MF10099
Registrant's Address : 36 Hoping Street, Louchu, Taoyuan 33842, Taiwan
Initial Date of Registration : 2020-08-05
Latest Date of Registration : 2020-08-05
Registration Number : 225MF10153
Registrant's Address : 1A, Sector 16A, Noida 201 301, Uttar Pradesh, India
Initial Date of Registration : 2013-08-09
Latest Date of Registration : 2014-11-17
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PharmaCompass offers a list of Linezolid 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 Linezolid manufacturer or Linezolid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Linezolid manufacturer or Linezolid supplier.
PharmaCompass also assists you with knowing the Linezolid API Price utilized in the formulation of products. Linezolid API Price is not always fixed or binding as the Linezolid Price is obtained through a variety of data sources. The Linezolid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A HSDB 7478 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of HSDB 7478, including repackagers and relabelers. The FDA regulates HSDB 7478 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. HSDB 7478 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 HSDB 7478 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A HSDB 7478 supplier is an individual or a company that provides HSDB 7478 active pharmaceutical ingredient (API) or HSDB 7478 finished formulations upon request. The HSDB 7478 suppliers may include HSDB 7478 API manufacturers, exporters, distributors and traders.
click here to find a list of HSDB 7478 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 HSDB 7478 Drug Master File in Japan (HSDB 7478 JDMF) empowers HSDB 7478 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 HSDB 7478 JDMF during the approval evaluation for pharmaceutical products. At the time of HSDB 7478 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 HSDB 7478 suppliers with JDMF on PharmaCompass.
We have 3 companies offering HSDB 7478
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