01 1Divi's Laboratories Limited
02 1Zhejiang Haizhou Pharmaceutical Co., Ltd.
03 1Zhejiang Starry Pharmaceutical Co., Ltd.
01 3Iohexol
01 2China
02 1India
NDC Package Code : 62331-066
Start Marketing Date : 2022-07-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65072-0801
Start Marketing Date : 2020-07-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 43228-100
Start Marketing Date : 1985-12-26
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing OMNIPAQUE 350 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for OMNIPAQUE 350 API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture OMNIPAQUE 350 as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain OMNIPAQUE 350 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a OMNIPAQUE 350 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of OMNIPAQUE 350 suppliers with NDC on PharmaCompass.
We have 3 companies offering OMNIPAQUE 350
Get in contact with the supplier of your choice:
