01 1Ocean NanoTech
01 1IRON OXIDE NANOPARTICLES FOR TARGETED DRUG DELIVERY
01 1U.S.A
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 29319
Submission : 2015-04-28
Status : Active
Type : IV
A Iron monooxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iron monooxide, including repackagers and relabelers. The FDA regulates Iron monooxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iron monooxide 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 Iron monooxide supplier is an individual or a company that provides Iron monooxide active pharmaceutical ingredient (API) or Iron monooxide finished formulations upon request. The Iron monooxide suppliers may include Iron monooxide API manufacturers, exporters, distributors and traders.
click here to find a list of Iron monooxide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Iron monooxide DMF (Drug Master File) is a document detailing the whole manufacturing process of Iron monooxide active pharmaceutical ingredient (API) in detail. Different forms of Iron monooxide DMFs exist exist since differing nations have different regulations, such as Iron monooxide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Iron monooxide DMF submitted to regulatory agencies in the US is known as a USDMF. Iron monooxide USDMF includes data on Iron monooxide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Iron monooxide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Iron monooxide suppliers with USDMF on PharmaCompass.
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