01 1BASF Corporation
02 1Hubei Biocause Heilen Pharmaceutical Co., Ltd
03 1SMS Pharmaceuticals Limited
04 1SOLARA ACTIVE PHARMA SCIENCES LIMITED
05 1Shandong Xinhua Pharmaceutical Company Limited
01 2Ibuprofen Sodium
02 1Ibuprofen Sodium Dihydrate
03 1Ibuprofen sodium dihydrate
04 1Sodium Ibuprofen Dihydrate
01 2China
02 1Germany
03 2India
NDC Package Code : 10117-0990
Start Marketing Date : 2005-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62068-110
Start Marketing Date : 2013-10-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 58624-0536
Start Marketing Date : 2010-06-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 67835-0032
Start Marketing Date : 2024-06-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 72643-040
Start Marketing Date : 2025-03-03
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Ibuprofen Sodium 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 Ibuprofen Sodium manufacturer or Ibuprofen Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Ibuprofen Sodium API Price utilized in the formulation of products. Ibuprofen Sodium API Price is not always fixed or binding as the Ibuprofen Sodium Price is obtained through a variety of data sources. The Ibuprofen Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A sodium 2-[4-(2-methylpropyl)phenyl]propanoate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of sodium 2-[4-(2-methylpropyl)phenyl]propanoate, including repackagers and relabelers. The FDA regulates sodium 2-[4-(2-methylpropyl)phenyl]propanoate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. sodium 2-[4-(2-methylpropyl)phenyl]propanoate 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 sodium 2-[4-(2-methylpropyl)phenyl]propanoate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A sodium 2-[4-(2-methylpropyl)phenyl]propanoate supplier is an individual or a company that provides sodium 2-[4-(2-methylpropyl)phenyl]propanoate active pharmaceutical ingredient (API) or sodium 2-[4-(2-methylpropyl)phenyl]propanoate finished formulations upon request. The sodium 2-[4-(2-methylpropyl)phenyl]propanoate suppliers may include sodium 2-[4-(2-methylpropyl)phenyl]propanoate API manufacturers, exporters, distributors and traders.
click here to find a list of sodium 2-[4-(2-methylpropyl)phenyl]propanoate 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 sodium 2-[4-(2-methylpropyl)phenyl]propanoate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for sodium 2-[4-(2-methylpropyl)phenyl]propanoate 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 sodium 2-[4-(2-methylpropyl)phenyl]propanoate 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 sodium 2-[4-(2-methylpropyl)phenyl]propanoate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a sodium 2-[4-(2-methylpropyl)phenyl]propanoate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of sodium 2-[4-(2-methylpropyl)phenyl]propanoate suppliers with NDC on PharmaCompass.
We have 5 companies offering sodium 2-[4-(2-methylpropyl)phenyl]propanoate
Get in contact with the supplier of your choice:
