01 1Divis Laboratories
02 1Hovione
03 1Interpharma Praha AS
04 2Zhejiang Starry Pharmaceutical Co., Ltd
01 3IOHEXOL
02 1IOHEXOL DRUG SUBSTANCE, FOR ORAL PRODUCTS
03 1IOHEXOL USP
01 2China
02 1Czech Republic
03 1India
04 1Portugal
01 2Active
02 3Inactive
01 2Complete
02 3Blank
GDUFA
DMF Review : Complete
Rev. Date : 2023-05-03
Pay. Date : 2023-03-23
DMF Number : 38195
Submission : 2023-03-20
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23148
Submission : 2009-10-02
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26641
Submission : 2013-01-24
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2021-10-13
Pay. Date : 2021-09-14
DMF Number : 36038
Submission : 2021-09-15
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22535
Submission : 2009-02-23
Status : Inactive
Type : II
27
PharmaCompass offers a list of Iohexol 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 Iohexol manufacturer or Iohexol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Iohexol manufacturer or Iohexol supplier.
PharmaCompass also assists you with knowing the Iohexol API Price utilized in the formulation of products. Iohexol API Price is not always fixed or binding as the Iohexol Price is obtained through a variety of data sources. The Iohexol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A OMNIPAQUE 350 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of OMNIPAQUE 350, including repackagers and relabelers. The FDA regulates OMNIPAQUE 350 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. OMNIPAQUE 350 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 OMNIPAQUE 350 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A OMNIPAQUE 350 supplier is an individual or a company that provides OMNIPAQUE 350 active pharmaceutical ingredient (API) or OMNIPAQUE 350 finished formulations upon request. The OMNIPAQUE 350 suppliers may include OMNIPAQUE 350 API manufacturers, exporters, distributors and traders.
click here to find a list of OMNIPAQUE 350 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A OMNIPAQUE 350 DMF (Drug Master File) is a document detailing the whole manufacturing process of OMNIPAQUE 350 active pharmaceutical ingredient (API) in detail. Different forms of OMNIPAQUE 350 DMFs exist exist since differing nations have different regulations, such as OMNIPAQUE 350 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A OMNIPAQUE 350 DMF submitted to regulatory agencies in the US is known as a USDMF. OMNIPAQUE 350 USDMF includes data on OMNIPAQUE 350's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The OMNIPAQUE 350 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of OMNIPAQUE 350 suppliers with USDMF on PharmaCompass.
We have 4 companies offering OMNIPAQUE 350
Get in contact with the supplier of your choice:
