01 1Wuxi Fortune Pharmaceutical Co., Ltd
01 1CANTHARIDIN
01 1China
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37369
Submission : 2023-04-14
Status : Active
Type : II
A Cantharidin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cantharidin, including repackagers and relabelers. The FDA regulates Cantharidin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cantharidin 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 Cantharidin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cantharidin supplier is an individual or a company that provides Cantharidin active pharmaceutical ingredient (API) or Cantharidin finished formulations upon request. The Cantharidin suppliers may include Cantharidin API manufacturers, exporters, distributors and traders.
click here to find a list of Cantharidin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cantharidin DMF (Drug Master File) is a document detailing the whole manufacturing process of Cantharidin active pharmaceutical ingredient (API) in detail. Different forms of Cantharidin DMFs exist exist since differing nations have different regulations, such as Cantharidin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cantharidin DMF submitted to regulatory agencies in the US is known as a USDMF. Cantharidin USDMF includes data on Cantharidin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cantharidin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cantharidin suppliers with USDMF on PharmaCompass.
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