01 1Aurobindo Pharma Limited
02 1Syn-Tech Chem. & Pharm. Co. , Ltd.
01 1Amorphous atorvastatin calcium
02 1Oxazolam
01 1India
02 1Taiwan
Amorphous Atorvastatin Calcium
Registration Number : 223MF10105
Registrant's Address : Plot No. 2, Maitrivihar, Ameerpet, Hyderabad Telangana, India
Initial Date of Registration : 2011-07-15
Latest Date of Registration : 2011-07-15
Registration Number : 224MF10023
Registrant's Address : No. 168 Kai-Yuan Rd. , Hsin-Ying Tainan City, 73055. Taiwan
Initial Date of Registration : 2012-02-01
Latest Date of Registration : 2022-08-03
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PharmaCompass offers a list of Oxazolam API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Oxazolam manufacturer or Oxazolam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxazolam manufacturer or Oxazolam supplier.
PharmaCompass also assists you with knowing the Oxazolam API Price utilized in the formulation of products. Oxazolam API Price is not always fixed or binding as the Oxazolam Price is obtained through a variety of data sources. The Oxazolam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oxazolam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxazolam, including repackagers and relabelers. The FDA regulates Oxazolam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxazolam API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Oxazolam supplier is an individual or a company that provides Oxazolam active pharmaceutical ingredient (API) or Oxazolam finished formulations upon request. The Oxazolam suppliers may include Oxazolam API manufacturers, exporters, distributors and traders.
click here to find a list of Oxazolam 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 Oxazolam Drug Master File in Japan (Oxazolam JDMF) empowers Oxazolam 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 Oxazolam JDMF during the approval evaluation for pharmaceutical products. At the time of Oxazolam 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 Oxazolam suppliers with JDMF on PharmaCompass.
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