01 1Arch Pharmalabs Limited
02 1Watson Pharma Private Limited
01 2Piroxicam
01 1India
02 1Ireland
Registration Number : 220MF10258
Registrant's Address : 201/301, Corporate Enclave, HDO-Corporate Building, Wing'B', B. D. Sawant Marg, Chaka...
Initial Date of Registration : 2008-12-22
Latest Date of Registration : 2008-12-22
Registration Number : 221MF10166
Registrant's Address : 505 Hyde Park, Chandivali Junction, Saki Vihar Road, Andheri East, Mumbai 400072, Mah...
Initial Date of Registration : 2009-07-30
Latest Date of Registration : 2009-07-30
A Piroxicam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Piroxicam, including repackagers and relabelers. The FDA regulates Piroxicam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Piroxicam 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 Piroxicam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Piroxicam supplier is an individual or a company that provides Piroxicam active pharmaceutical ingredient (API) or Piroxicam finished formulations upon request. The Piroxicam suppliers may include Piroxicam API manufacturers, exporters, distributors and traders.
click here to find a list of Piroxicam 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 Piroxicam Drug Master File in Japan (Piroxicam JDMF) empowers Piroxicam 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 Piroxicam JDMF during the approval evaluation for pharmaceutical products. At the time of Piroxicam 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 Piroxicam suppliers with JDMF on PharmaCompass.
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