01 1Angelini Pharma
01 1ETOPERIDONE HYDROCHLORIDE
01 1Italy
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8372
Submission : 1989-11-22
Status : Inactive
Type : II
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PharmaCompass offers a list of Etoperidone Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Etoperidone Hydrochloride manufacturer or Etoperidone Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Etoperidone Hydrochloride manufacturer or Etoperidone Hydrochloride supplier.
PharmaCompass also assists you with knowing the Etoperidone Hydrochloride API Price utilized in the formulation of products. Etoperidone Hydrochloride API Price is not always fixed or binding as the Etoperidone Hydrochloride Price is obtained through a variety of data sources. The Etoperidone Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Etonin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etonin, including repackagers and relabelers. The FDA regulates Etonin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etonin 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 Etonin supplier is an individual or a company that provides Etonin active pharmaceutical ingredient (API) or Etonin finished formulations upon request. The Etonin suppliers may include Etonin API manufacturers, exporters, distributors and traders.
click here to find a list of Etonin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Etonin DMF (Drug Master File) is a document detailing the whole manufacturing process of Etonin active pharmaceutical ingredient (API) in detail. Different forms of Etonin DMFs exist exist since differing nations have different regulations, such as Etonin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Etonin DMF submitted to regulatory agencies in the US is known as a USDMF. Etonin USDMF includes data on Etonin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Etonin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Etonin suppliers with USDMF on PharmaCompass.
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