01 1BASF Corporation
02 1Hubei Biocause Heilen Pharmaceutical Co., Ltd
03 1SMS Pharmaceuticals Limited
04 1Shandong Xinhua Pharmaceutical Company Limited
01 2Ibuprofen Sodium
02 1Ibuprofen Sodium Dihydrate
03 1Sodium Ibuprofen Dihydrate
01 2China
02 1Germany
03 1India
NDC Package Code : 10117-0990
Start Marketing Date : 2005-04-01
End Marketing Date : 2024-12-31
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
A Ibuprofen Sodium Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ibuprofen Sodium Dihydrate, including repackagers and relabelers. The FDA regulates Ibuprofen Sodium Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ibuprofen Sodium Dihydrate 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 Ibuprofen Sodium Dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ibuprofen Sodium Dihydrate supplier is an individual or a company that provides Ibuprofen Sodium Dihydrate active pharmaceutical ingredient (API) or Ibuprofen Sodium Dihydrate finished formulations upon request. The Ibuprofen Sodium Dihydrate suppliers may include Ibuprofen Sodium Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Ibuprofen Sodium Dihydrate 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 Ibuprofen Sodium Dihydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ibuprofen Sodium Dihydrate 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 Ibuprofen Sodium Dihydrate 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 Ibuprofen Sodium Dihydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ibuprofen Sodium Dihydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ibuprofen Sodium Dihydrate suppliers with NDC on PharmaCompass.
We have 4 companies offering Ibuprofen Sodium Dihydrate
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