Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1Aarti Pharmalabs
02 1Apotex Pharmachem
03 1Emcure Pharmaceuticals
04 1Katwijk Chemie
05 1Taro Pharmaceutical Industries
06 1Zydus Lifesciences
01 11,2-DIMETHYL-3-HYDROXY-PYRIDONE-4 (DEFERIPRONE)
02 5DEFERIPRONE
01 1Canada
02 3India
03 1Netherlands
04 1U.S.A
01 5Active
02 1Inactive
01 2Complete
02 4Blank
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39766
Submission : 2024-04-16
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10867
Submission : 1994-04-12
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21640
Submission : 2008-05-19
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2019-10-16
Pay. Date : 2019-09-25
DMF Number : 14335
Submission : 1999-08-06
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-06-09
Pay. Date : 2015-03-31
DMF Number : 28983
Submission : 2015-03-30
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14910
Submission : 2000-06-01
Status : Inactive
Type : II
A Ferriprox manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ferriprox, including repackagers and relabelers. The FDA regulates Ferriprox manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ferriprox 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 Ferriprox supplier is an individual or a company that provides Ferriprox active pharmaceutical ingredient (API) or Ferriprox finished formulations upon request. The Ferriprox suppliers may include Ferriprox API manufacturers, exporters, distributors and traders.
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A Ferriprox DMF (Drug Master File) is a document detailing the whole manufacturing process of Ferriprox active pharmaceutical ingredient (API) in detail. Different forms of Ferriprox DMFs exist exist since differing nations have different regulations, such as Ferriprox USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ferriprox DMF submitted to regulatory agencies in the US is known as a USDMF. Ferriprox USDMF includes data on Ferriprox's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ferriprox USDMF is kept confidential to protect the manufacturer’s intellectual property.
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