01 1Hubei Gedian Humanwell Pharmaceutical
01 1CASTOR OIL REFINED
01 1China
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34542
Submission : 2020-12-17
Status : Active
Type : IV
A Venelex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Venelex, including repackagers and relabelers. The FDA regulates Venelex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Venelex API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Venelex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Venelex supplier is an individual or a company that provides Venelex active pharmaceutical ingredient (API) or Venelex finished formulations upon request. The Venelex suppliers may include Venelex API manufacturers, exporters, distributors and traders.
click here to find a list of Venelex suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Venelex DMF (Drug Master File) is a document detailing the whole manufacturing process of Venelex active pharmaceutical ingredient (API) in detail. Different forms of Venelex DMFs exist exist since differing nations have different regulations, such as Venelex USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Venelex DMF submitted to regulatory agencies in the US is known as a USDMF. Venelex USDMF includes data on Venelex's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Venelex USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Venelex suppliers with USDMF on PharmaCompass.
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