01 1Ipca Laboratories Limited
02 1Syn-Tech Chem. & Pharm. Co. , Ltd.
01 1Atenolol
02 1Atenolol (production only)
01 1India
02 1Taiwan
Registration Number : 218MF10439
Registrant's Address : 48, Kandivli Industrial Estate, Kandivli (W), Mumbai 400 067, India
Initial Date of Registration : 2006-04-27
Latest Date of Registration : 2024-02-07
Atenolol (for manufacturing purposes only)
Registration Number : 222MF10107
Registrant's Address : No. 168 Kai-Yuan Rd. , Hsin-Ying Tainan City, 73055. Taiwan
Initial Date of Registration : 2010-03-23
Latest Date of Registration : 2010-03-23
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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, and more, enabling you to easily find the right Atenolol manufacturer or Atenolol supplier for your needs.
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A Atenol Nordic manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Atenol Nordic, including repackagers and relabelers. The FDA regulates Atenol Nordic manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Atenol Nordic 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 Atenol Nordic manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Atenol Nordic supplier is an individual or a company that provides Atenol Nordic active pharmaceutical ingredient (API) or Atenol Nordic finished formulations upon request. The Atenol Nordic suppliers may include Atenol Nordic API manufacturers, exporters, distributors and traders.
click here to find a list of Atenol Nordic suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Atenol Nordic Drug Master File in Japan (Atenol Nordic JDMF) empowers Atenol Nordic 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 Atenol Nordic JDMF during the approval evaluation for pharmaceutical products. At the time of Atenol Nordic 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 Atenol Nordic suppliers with JDMF on PharmaCompass.
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