01 1Hetero Labs Limited
02 1Jiangsu Hengrui Pharmaceuticals Co. , Ltd.
03 1Natco Pharma Limited.
04 1ScinoPharm Taiwan, Ltd.
05 1Shilpa Pharma Lifesciences Limited
06 1Synthimed Labs Private Limited
07 1Viyash Life Sciences Private Limited
01 7Letrozole
01 1China
02 5India
03 1Taiwan
Registration Number : 226MF10028
Registrant's Address : 7-2-A2,Hetero Corporate,Industrial Estates Sanath Nagar,Hyderabad-500 018 Telangana I...
Initial Date of Registration : 2014-02-05
Latest Date of Registration : 2014-02-05
Registration Number : 226MF10023
Registrant's Address : Village-Bhagwanpur, Barwala Road, Derabassi-140 507 District-S. A. S. Nagar (Mohali)P...
Initial Date of Registration : 2014-01-21
Latest Date of Registration : 2014-11-17
Registration Number : 226MF10030
Registrant's Address : No. 7, Kunlunshan Road, Economic and Technological Development Zone, Lianyungang, Jia...
Initial Date of Registration : 2014-02-05
Latest Date of Registration : 2014-02-05
Registration Number : 226MF10005
Registrant's Address : Natco House, Road No. 2, Banjara Hills,Hyderabad 500034, Telangana, India
Initial Date of Registration : 2014-01-08
Latest Date of Registration : 2014-11-17
Registration Number : 226MF10063
Registrant's Address : No. 1, Nan-Ke 8th Road, Shan-Hua, Tainan 741014, Taiwan
Initial Date of Registration : 2014-03-06
Latest Date of Registration : 2024-05-08
Registration Number : 226MF10029
Registrant's Address : Shilpa House, #12-6-214/A1, Hyderabad Road, Raichur-584 135, Karnataka, India
Initial Date of Registration : 2014-02-05
Latest Date of Registration : 2015-04-21
Registration Number : 306MF10027
Registrant's Address : Plot No. 290, Srivalli's Corporate, Road No. 6, Kakatiya Hills, Madhapur, Hyderabad-5...
Initial Date of Registration : 2024-02-14
Latest Date of Registration : 2024-02-14
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PharmaCompass offers a list of Letrozole 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 Letrozole manufacturer or Letrozole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Letrozole manufacturer or Letrozole supplier.
PharmaCompass also assists you with knowing the Letrozole API Price utilized in the formulation of products. Letrozole API Price is not always fixed or binding as the Letrozole Price is obtained through a variety of data sources. The Letrozole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Femara manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Femara, including repackagers and relabelers. The FDA regulates Femara manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Femara 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 Femara manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Femara supplier is an individual or a company that provides Femara active pharmaceutical ingredient (API) or Femara finished formulations upon request. The Femara suppliers may include Femara API manufacturers, exporters, distributors and traders.
click here to find a list of Femara 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 Femara Drug Master File in Japan (Femara JDMF) empowers Femara 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 Femara JDMF during the approval evaluation for pharmaceutical products. At the time of Femara 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 Femara suppliers with JDMF on PharmaCompass.
We have 7 companies offering Femara
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