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01 1PENTEX HUMAN TRANSFERRIN, IRON SATURATED
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9256
Submission : 1991-07-24
Status : Inactive
Type : II
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PharmaCompass offers a list of Uric Acid 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 Uric Acid manufacturer or Uric Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Uric Acid manufacturer or Uric Acid supplier.
PharmaCompass also assists you with knowing the Uric Acid API Price utilized in the formulation of products. Uric Acid API Price is not always fixed or binding as the Uric Acid Price is obtained through a variety of data sources. The Uric Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Monosodium Urate Monohydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Monosodium Urate Monohydrate, including repackagers and relabelers. The FDA regulates Monosodium Urate Monohydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Monosodium Urate Monohydrate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Monosodium Urate Monohydrate supplier is an individual or a company that provides Monosodium Urate Monohydrate active pharmaceutical ingredient (API) or Monosodium Urate Monohydrate finished formulations upon request. The Monosodium Urate Monohydrate suppliers may include Monosodium Urate Monohydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Monosodium Urate Monohydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Monosodium Urate Monohydrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Monosodium Urate Monohydrate active pharmaceutical ingredient (API) in detail. Different forms of Monosodium Urate Monohydrate DMFs exist exist since differing nations have different regulations, such as Monosodium Urate Monohydrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Monosodium Urate Monohydrate DMF submitted to regulatory agencies in the US is known as a USDMF. Monosodium Urate Monohydrate USDMF includes data on Monosodium Urate Monohydrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Monosodium Urate Monohydrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Monosodium Urate Monohydrate suppliers with USDMF on PharmaCompass.
