01 1Zhejiang Jianfeng Haizhou
01 1ACETOIODIDE
01 1China
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33239
Submission : 2018-10-28
Status : Active
Type : II
A Iodide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iodide, including repackagers and relabelers. The FDA regulates Iodide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iodide 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 Iodide supplier is an individual or a company that provides Iodide active pharmaceutical ingredient (API) or Iodide finished formulations upon request. The Iodide suppliers may include Iodide API manufacturers, exporters, distributors and traders.
click here to find a list of Iodide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Iodide DMF (Drug Master File) is a document detailing the whole manufacturing process of Iodide active pharmaceutical ingredient (API) in detail. Different forms of Iodide DMFs exist exist since differing nations have different regulations, such as Iodide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Iodide DMF submitted to regulatory agencies in the US is known as a USDMF. Iodide USDMF includes data on Iodide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Iodide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Iodide suppliers with USDMF on PharmaCompass.
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