01 1Ashland Inc.
02 1BASF Corporation
03 1Glide Chem Pvt. Ltd.
04 1Marcus Research Laboratory, Inc.
01 1Day stations povidone-iodine (production only)
02 1PVP IODINE
03 1Povidone-iodine PVP-IODINE
04 1Povidone-iodine PVP-Iodine
01 1Germany
02 1India
03 2U.S.A
Registration Number : 218MF10438
Registrant's Address : 8145 Blazer Drive, Wilmington, DE, 19808, United States
Initial Date of Registration : 2006-04-27
Latest Date of Registration : 2024-05-29
Registration Number : 217MF10985
Registrant's Address : 100 Park Avenue, Florham Park, New Jersey, 07932, United States of America
Initial Date of Registration : 2005-11-21
Latest Date of Registration : 2016-05-17
Registration Number : 229MF10087
Registrant's Address : S-39, Rajouri Garden, New Delhi-110027, India
Initial Date of Registration : 2017-04-25
Latest Date of Registration : 2017-04-25
Japanese Pharmacopoeia Povidone-Iodine (for manufacturing purposes only)
Registration Number : 218MF10060
Registrant's Address : 1820 Delmar Blvd. , St. Louis, MO 63103, USA
Initial Date of Registration : 2006-01-27
Latest Date of Registration : 2010-03-19
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PharmaCompass offers a list of Povidone Iodine 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 Povidone Iodine manufacturer or Povidone Iodine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Povidone Iodine manufacturer or Povidone Iodine supplier.
PharmaCompass also assists you with knowing the Povidone Iodine API Price utilized in the formulation of products. Povidone Iodine API Price is not always fixed or binding as the Povidone Iodine Price is obtained through a variety of data sources. The Povidone Iodine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bridine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bridine, including repackagers and relabelers. The FDA regulates Bridine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bridine 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 Bridine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bridine supplier is an individual or a company that provides Bridine active pharmaceutical ingredient (API) or Bridine finished formulations upon request. The Bridine suppliers may include Bridine API manufacturers, exporters, distributors and traders.
click here to find a list of Bridine 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 Bridine Drug Master File in Japan (Bridine JDMF) empowers Bridine 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 Bridine JDMF during the approval evaluation for pharmaceutical products. At the time of Bridine 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 Bridine suppliers with JDMF on PharmaCompass.
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