01 1Dupont
01 1SODIUM-24 RADIOISOTOPE (FORMERLY NEW ENGLAND NUCLEAR)
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2372
Submission : 1974-12-16
Status : Inactive
Type : II
A Sodium-24 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium-24, including repackagers and relabelers. The FDA regulates Sodium-24 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium-24 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 Sodium-24 supplier is an individual or a company that provides Sodium-24 active pharmaceutical ingredient (API) or Sodium-24 finished formulations upon request. The Sodium-24 suppliers may include Sodium-24 API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium-24 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sodium-24 DMF (Drug Master File) is a document detailing the whole manufacturing process of Sodium-24 active pharmaceutical ingredient (API) in detail. Different forms of Sodium-24 DMFs exist exist since differing nations have different regulations, such as Sodium-24 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sodium-24 DMF submitted to regulatory agencies in the US is known as a USDMF. Sodium-24 USDMF includes data on Sodium-24's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sodium-24 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sodium-24 suppliers with USDMF on PharmaCompass.
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