Axplora- The 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.
01 2Atenolol
02 1Atenolol "Teva / TPC"
03 1Atenolol "Teva"
04 1Atenolol (production only)
01 1Germany
02 1India
03 2Israel
04 1Taiwan
Axplora- The 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
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
A Tenormin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tenormin, including repackagers and relabelers. The FDA regulates Tenormin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tenormin 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 Tenormin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tenormin supplier is an individual or a company that provides Tenormin active pharmaceutical ingredient (API) or Tenormin finished formulations upon request. The Tenormin suppliers may include Tenormin API manufacturers, exporters, distributors and traders.
click here to find a list of Tenormin 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 Tenormin Drug Master File in Japan (Tenormin JDMF) empowers Tenormin 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 Tenormin JDMF during the approval evaluation for pharmaceutical products. At the time of Tenormin 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 Tenormin suppliers with JDMF on PharmaCompass.
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