01 1Sichuan Xieli Pharmaceutical
01 1INGENOL MEBUTATE
01 1China
01 1Active
01 1Complete
GDUFA
DMF Review : Complete
Rev. Date : 2015-12-23
Pay. Date : 2015-08-12
DMF Number : 29556
Submission : 2015-07-17
Status : Active
Type : II
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A picato manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of picato, including repackagers and relabelers. The FDA regulates picato manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. picato 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 picato manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A picato supplier is an individual or a company that provides picato active pharmaceutical ingredient (API) or picato finished formulations upon request. The picato suppliers may include picato API manufacturers, exporters, distributors and traders.
click here to find a list of picato suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A picato DMF (Drug Master File) is a document detailing the whole manufacturing process of picato active pharmaceutical ingredient (API) in detail. Different forms of picato DMFs exist exist since differing nations have different regulations, such as picato USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A picato DMF submitted to regulatory agencies in the US is known as a USDMF. picato USDMF includes data on picato's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The picato USDMF is kept confidential to protect the manufacturer’s intellectual property.
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