01 2Lundbeck Pharmaceuticals Italy S. p. A
02 1Lusochimica S. p. A.
01 3Ritodrine hydrochloride
01 2Denmark
02 1Italy
Registration Number : 218MF10513
Registrant's Address : Via Quarta Strada, 2 Padova ITALY
Initial Date of Registration : 2006-05-18
Latest Date of Registration : 2006-05-18
Registration Number : 224MF10226
Registrant's Address : Via Quarta Strada, 2 Padova, Italy
Initial Date of Registration : 2012-12-06
Latest Date of Registration : 2012-12-06
Registration Number : 217MF11180
Registrant's Address : Via Giotto 9,23871 Lomagna(LC)Italy
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2021-05-17
A Ritodrine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ritodrine Hydrochloride, including repackagers and relabelers. The FDA regulates Ritodrine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ritodrine Hydrochloride 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 Ritodrine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ritodrine Hydrochloride supplier is an individual or a company that provides Ritodrine Hydrochloride active pharmaceutical ingredient (API) or Ritodrine Hydrochloride finished formulations upon request. The Ritodrine Hydrochloride suppliers may include Ritodrine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Ritodrine Hydrochloride 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 Ritodrine Hydrochloride Drug Master File in Japan (Ritodrine Hydrochloride JDMF) empowers Ritodrine Hydrochloride 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 Ritodrine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Ritodrine Hydrochloride 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 Ritodrine Hydrochloride suppliers with JDMF on PharmaCompass.
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