Axplora is your partner of choice for complex APIs.
01 1PharmaZell (India) Private Limited
02 1Teva Pharmaceutical & Chemical (Hangzhou) Co. , Ltd.
03 1Teva Pharmaceuticals Fine Chemicals S. r. l.
04 1Ipca Laboratories Limited
05 1Syn-Tech Chem. & Pharm. Co. , Ltd.
Axplora is your partner of choice for complex APIs.
Registration Number : 220MF10018
Registrant's Address : Plot No. B5 & B6, MEPZ, Tambaram, Chennai 600 045, India
Initial Date of Registration : 2008-01-09
Latest Date of Registration : 2008-01-09
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registration Number : 227MF10251
Registrant's Address : No. 1889, Jingliu Road, Linjiang Industrial Zone, Qiantang New District, Hangzhou, Ch...
Initial Date of Registration : 2015-10-08
Latest Date of Registration : 2015-10-08
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registration Number : 218MF10719
Registrant's Address : Via Messina, 38, 20154 Milano Italy
Initial Date of Registration : 2006-09-06
Latest Date of Registration : 2006-09-06
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PharmaCompass offers a list of Atenolol 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 Atenolol manufacturer or Atenolol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Atenolol manufacturer or Atenolol supplier.
PharmaCompass also assists you with knowing the Atenolol API Price utilized in the formulation of products. Atenolol API Price is not always fixed or binding as the Atenolol Price is obtained through a variety of data sources. The Atenolol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Atenolol, analytical reference material manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Atenolol, analytical reference material, including repackagers and relabelers. The FDA regulates Atenolol, analytical reference material manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Atenolol, analytical reference material 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 Atenolol, analytical reference material manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Atenolol, analytical reference material supplier is an individual or a company that provides Atenolol, analytical reference material active pharmaceutical ingredient (API) or Atenolol, analytical reference material finished formulations upon request. The Atenolol, analytical reference material suppliers may include Atenolol, analytical reference material API manufacturers, exporters, distributors and traders.
click here to find a list of Atenolol, analytical reference material 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 Atenolol, analytical reference material Drug Master File in Japan (Atenolol, analytical reference material JDMF) empowers Atenolol, analytical reference material 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 Atenolol, analytical reference material JDMF during the approval evaluation for pharmaceutical products. At the time of Atenolol, analytical reference material 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 Atenolol, analytical reference material suppliers with JDMF on PharmaCompass.
We have 4 companies offering Atenolol, analytical reference material
Get in contact with the supplier of your choice:
