Lifecare Labs has been developing innovative products in specialist areas of medicine.
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01 1Vasudha Pharma Chem Limited
02 3CF Pharma Ltd.
03 1UBE Inc.
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01 2Biperiden Hydrochloride
02 1Biperiden base
03 1Biperiden hydrochloride
04 1Tasumorin
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01 3Hungary
02 1India
03 1Japan
Registration Number : 305MF10051
Registrant's Address : 78/A, Bengalrao Nagar, Hyderabad-500 038, Telangana State, India.
Initial Date of Registration : 2023-04-25
Latest Date of Registration : 2023-04-25
Registration Number : 217MF11000
Registrant's Address : 1978-96 Ogushi, Ube City, Yamaguchi Prefecture
Initial Date of Registration : 2005-11-21
Latest Date of Registration : 2013-08-14
Registration Number : 225MF10123
Registrant's Address : H-1097 Budapest, Ke(')n u. 5. Hungary
Initial Date of Registration : 2013-06-19
Latest Date of Registration : 2013-06-19
Registration Number : 304MF10066
Registrant's Address : H-1097 Budapest, Ke(')n u. 5. Hungary
Initial Date of Registration : 2022-04-13
Latest Date of Registration : 2022-04-13
Registration Number : 304MF10057
Registrant's Address : H-1097 Budapest, Ke(')n u. 5. Hungary
Initial Date of Registration : 2022-03-24
Latest Date of Registration : 2022-03-24
A Biperiden manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Biperiden, including repackagers and relabelers. The FDA regulates Biperiden manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Biperiden 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 Biperiden manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Biperiden supplier is an individual or a company that provides Biperiden active pharmaceutical ingredient (API) or Biperiden finished formulations upon request. The Biperiden suppliers may include Biperiden API manufacturers, exporters, distributors and traders.
click here to find a list of Biperiden 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 Biperiden Drug Master File in Japan (Biperiden JDMF) empowers Biperiden 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 Biperiden JDMF during the approval evaluation for pharmaceutical products. At the time of Biperiden 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 Biperiden suppliers with JDMF on PharmaCompass.
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