Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1Biophore India Pharmaceuticals Pvt Ltd
02 1Curia
03 1Honour Lab
04 1ORGANICA Feinchemie GmbH Wolfen
05 1Vasudha Pharma Chem
01 2DIATRIZOATE MEGLUMINE
02 2DIATRIZOATE MEGLUMINE USP
03 1DIATRIZOATE MEGLUMINE, USP
01 1Germany
02 3India
03 1U.S.A
01 4Active
02 1Inactive
01 3Complete
02 2Blank
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : Complete
Rev. Date : 2015-08-05
Pay. Date : 2015-04-08
DMF Number : 28740
Submission : 2014-10-31
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-04-25
Pay. Date : 2013-05-21
DMF Number : 27165
Submission : 2013-05-22
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2020-04-24
Pay. Date : 2020-01-09
DMF Number : 34403
Submission : 2020-04-09
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4686
Submission : 1982-10-15
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32737
Submission : 2018-07-25
Status : Active
Type : II
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PharmaCompass offers a list of Diatrizoate Meglumine 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 Diatrizoate Meglumine manufacturer or Diatrizoate Meglumine supplier for your needs.
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PharmaCompass also assists you with knowing the Diatrizoate Meglumine API Price utilized in the formulation of products. Diatrizoate Meglumine API Price is not always fixed or binding as the Diatrizoate Meglumine Price is obtained through a variety of data sources. The Diatrizoate Meglumine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Urografin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Urografin, including repackagers and relabelers. The FDA regulates Urografin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Urografin 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 Urografin supplier is an individual or a company that provides Urografin active pharmaceutical ingredient (API) or Urografin finished formulations upon request. The Urografin suppliers may include Urografin API manufacturers, exporters, distributors and traders.
click here to find a list of Urografin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Urografin DMF (Drug Master File) is a document detailing the whole manufacturing process of Urografin active pharmaceutical ingredient (API) in detail. Different forms of Urografin DMFs exist exist since differing nations have different regulations, such as Urografin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Urografin DMF submitted to regulatory agencies in the US is known as a USDMF. Urografin USDMF includes data on Urografin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Urografin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Urografin suppliers with USDMF on PharmaCompass.
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