01 13M Company
01 1ADRENALONE HYDROCHLORIDE
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3859
Submission : 1980-07-04
Status : Inactive
Type : II
A Adrenalone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Adrenalone, including repackagers and relabelers. The FDA regulates Adrenalone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Adrenalone 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 Adrenalone supplier is an individual or a company that provides Adrenalone active pharmaceutical ingredient (API) or Adrenalone finished formulations upon request. The Adrenalone suppliers may include Adrenalone API manufacturers, exporters, distributors and traders.
click here to find a list of Adrenalone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Adrenalone DMF (Drug Master File) is a document detailing the whole manufacturing process of Adrenalone active pharmaceutical ingredient (API) in detail. Different forms of Adrenalone DMFs exist exist since differing nations have different regulations, such as Adrenalone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Adrenalone DMF submitted to regulatory agencies in the US is known as a USDMF. Adrenalone USDMF includes data on Adrenalone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Adrenalone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Adrenalone suppliers with USDMF on PharmaCompass.
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