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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 40941
Submission : 2024-12-30
Status : Active
Type : II
Certificate Number : CEP 2025-012 - Rev 00
Issue Date : 2025-07-22
Type : Chemical
Substance Number : 1142
Status : Valid
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33462
Submission : 2018-12-28
Status : Active
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22686
Submission : 2009-04-01
Status : Active
Type : II
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 :
NDC Package Code : 44242-100
Start Marketing Date : 1981-04-02
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 183
Submission : 1952-02-29
Status : Active
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36110
Submission : 2021-07-14
Status : Active
Type : II
Certificate Number : R1-CEP 2016-046 - Rev 00
Issue Date : 2021-05-05
Type : Chemical
Substance Number : 685
Status : Valid

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3017
Submission : 1977-07-22
Status : Active
Type : II
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 :
NDC Package Code : 70177-0002
Start Marketing Date : 2010-01-11
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33619
Submission : 2019-04-02
Status : Active
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20921
Submission : 2007-10-09
Status : Inactive
Type : II

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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, 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.
A Proviodine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Proviodine, including repackagers and relabelers. The FDA regulates Proviodine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Proviodine 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 Proviodine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Proviodine supplier is an individual or a company that provides Proviodine active pharmaceutical ingredient (API) or Proviodine finished formulations upon request. The Proviodine suppliers may include Proviodine API manufacturers, exporters, distributors and traders.
click here to find a list of Proviodine suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
We have 36 companies offering Proviodine
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