01 1Aurobindo Pharma Limited
01 1Pivmecillinam hydrochloride
01 1India
Registration Number : 220MF10224
Registrant's Address : Plot No. 2, Maitrivihar, Ameerprt, Hyderabad, Andhra Pradesh, India 500-038
Initial Date of Registration : 2008-11-10
Latest Date of Registration : 2008-11-10
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PharmaCompass offers a list of Pivmecillinam 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 Pivmecillinam manufacturer or Pivmecillinam supplier for your needs.
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PharmaCompass also assists you with knowing the Pivmecillinam API Price utilized in the formulation of products. Pivmecillinam API Price is not always fixed or binding as the Pivmecillinam Price is obtained through a variety of data sources. The Pivmecillinam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Coactabs (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Coactabs (TN), including repackagers and relabelers. The FDA regulates Coactabs (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Coactabs (TN) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Coactabs (TN) supplier is an individual or a company that provides Coactabs (TN) active pharmaceutical ingredient (API) or Coactabs (TN) finished formulations upon request. The Coactabs (TN) suppliers may include Coactabs (TN) API manufacturers, exporters, distributors and traders.
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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 Coactabs (TN) Drug Master File in Japan (Coactabs (TN) JDMF) empowers Coactabs (TN) 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 Coactabs (TN) JDMF during the approval evaluation for pharmaceutical products. At the time of Coactabs (TN) JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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