01 1SIGMA TAU
01 1ANGIOTENSIN I
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4479
Submission : 1982-03-24
Status : Inactive
Type : II
A Angiotensinogen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Angiotensinogen, including repackagers and relabelers. The FDA regulates Angiotensinogen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Angiotensinogen 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 Angiotensinogen supplier is an individual or a company that provides Angiotensinogen active pharmaceutical ingredient (API) or Angiotensinogen finished formulations upon request. The Angiotensinogen suppliers may include Angiotensinogen API manufacturers, exporters, distributors and traders.
click here to find a list of Angiotensinogen suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Angiotensinogen DMF (Drug Master File) is a document detailing the whole manufacturing process of Angiotensinogen active pharmaceutical ingredient (API) in detail. Different forms of Angiotensinogen DMFs exist exist since differing nations have different regulations, such as Angiotensinogen USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Angiotensinogen DMF submitted to regulatory agencies in the US is known as a USDMF. Angiotensinogen USDMF includes data on Angiotensinogen's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Angiotensinogen USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Angiotensinogen suppliers with USDMF on PharmaCompass.
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