01 1Zambon Group SpA
01 1ANA 756
01 1Italy
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11166
Submission : 1994-10-12
Status : Inactive
Type : II
A Tasosartan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tasosartan, including repackagers and relabelers. The FDA regulates Tasosartan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tasosartan 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 Tasosartan supplier is an individual or a company that provides Tasosartan active pharmaceutical ingredient (API) or Tasosartan finished formulations upon request. The Tasosartan suppliers may include Tasosartan API manufacturers, exporters, distributors and traders.
click here to find a list of Tasosartan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tasosartan DMF (Drug Master File) is a document detailing the whole manufacturing process of Tasosartan active pharmaceutical ingredient (API) in detail. Different forms of Tasosartan DMFs exist exist since differing nations have different regulations, such as Tasosartan USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tasosartan DMF submitted to regulatory agencies in the US is known as a USDMF. Tasosartan USDMF includes data on Tasosartan's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tasosartan USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tasosartan suppliers with USDMF on PharmaCompass.
We have 1 companies offering Tasosartan
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?