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
A Povidone-Iodine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Povidone-Iodine, including repackagers and relabelers. The FDA regulates Povidone-Iodine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Povidone-Iodine 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 Povidone-Iodine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Povidone-Iodine supplier is an individual or a company that provides Povidone-Iodine active pharmaceutical ingredient (API) or Povidone-Iodine finished formulations upon request. The Povidone-Iodine suppliers may include Povidone-Iodine API manufacturers, exporters, distributors and traders.
click here to find a list of Povidone-Iodine 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 Povidone-Iodine Drug Master File in Japan (Povidone-Iodine JDMF) empowers Povidone-Iodine 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 Povidone-Iodine JDMF during the approval evaluation for pharmaceutical products. At the time of Povidone-Iodine 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 Povidone-Iodine suppliers with JDMF on PharmaCompass.
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