01 1Zhejiang Hisun Pharmaceutical
01 1FR179642
01 1China
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 27434
Submission : 2013-08-29
Status : Active
Type : II
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A FR-179642 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of FR-179642, including repackagers and relabelers. The FDA regulates FR-179642 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. FR-179642 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 FR-179642 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A FR-179642 supplier is an individual or a company that provides FR-179642 active pharmaceutical ingredient (API) or FR-179642 finished formulations upon request. The FR-179642 suppliers may include FR-179642 API manufacturers, exporters, distributors and traders.
click here to find a list of FR-179642 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A FR-179642 DMF (Drug Master File) is a document detailing the whole manufacturing process of FR-179642 active pharmaceutical ingredient (API) in detail. Different forms of FR-179642 DMFs exist exist since differing nations have different regulations, such as FR-179642 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A FR-179642 DMF submitted to regulatory agencies in the US is known as a USDMF. FR-179642 USDMF includes data on FR-179642's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The FR-179642 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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