01 1Esteve Quimica
01 1ADATANSERIN HYDROCHLORIDE (CRUDE)
01 1Spain
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15823
Submission : 2002-01-24
Status : Inactive
Type : II
A Wy 50324 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Wy 50324, including repackagers and relabelers. The FDA regulates Wy 50324 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Wy 50324 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 Wy 50324 supplier is an individual or a company that provides Wy 50324 active pharmaceutical ingredient (API) or Wy 50324 finished formulations upon request. The Wy 50324 suppliers may include Wy 50324 API manufacturers, exporters, distributors and traders.
click here to find a list of Wy 50324 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Wy 50324 DMF (Drug Master File) is a document detailing the whole manufacturing process of Wy 50324 active pharmaceutical ingredient (API) in detail. Different forms of Wy 50324 DMFs exist exist since differing nations have different regulations, such as Wy 50324 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Wy 50324 DMF submitted to regulatory agencies in the US is known as a USDMF. Wy 50324 USDMF includes data on Wy 50324's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Wy 50324 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Wy 50324 suppliers with USDMF on PharmaCompass.
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