01 1Excella GmbH & Co. K.G.
02 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
01 2Haloperidol
01 1Italy
02 1Luxembourg
Registration Number : 221MF10041
Registrant's Address : NUERNBERGER STRASSE 12, 90537 FEUCHT, GERMANY
Initial Date of Registration : 2009-02-23
Latest Date of Registration : 2021-11-02
Registration Number : 219MF10333
Registrant's Address : Piazzale Luigi Cadorna, 4 - 20123 MILANO, Italy
Initial Date of Registration : 2007-11-20
Latest Date of Registration : 2019-06-25
A Haloperidol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Haloperidol, including repackagers and relabelers. The FDA regulates Haloperidol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Haloperidol 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 Haloperidol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Haloperidol supplier is an individual or a company that provides Haloperidol active pharmaceutical ingredient (API) or Haloperidol finished formulations upon request. The Haloperidol suppliers may include Haloperidol API manufacturers, exporters, distributors and traders.
click here to find a list of Haloperidol 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 Haloperidol Drug Master File in Japan (Haloperidol JDMF) empowers Haloperidol 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 Haloperidol JDMF during the approval evaluation for pharmaceutical products. At the time of Haloperidol 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 Haloperidol suppliers with JDMF on PharmaCompass.
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