01 1RP SCHERER GMBH & CO. KG
01 1MCN-5691
01 1Germany
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7112
Submission : 1987-04-30
Status : Inactive
Type : II
A Mcn-5691 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mcn-5691, including repackagers and relabelers. The FDA regulates Mcn-5691 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mcn-5691 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 Mcn-5691 supplier is an individual or a company that provides Mcn-5691 active pharmaceutical ingredient (API) or Mcn-5691 finished formulations upon request. The Mcn-5691 suppliers may include Mcn-5691 API manufacturers, exporters, distributors and traders.
click here to find a list of Mcn-5691 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Mcn-5691 DMF (Drug Master File) is a document detailing the whole manufacturing process of Mcn-5691 active pharmaceutical ingredient (API) in detail. Different forms of Mcn-5691 DMFs exist exist since differing nations have different regulations, such as Mcn-5691 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Mcn-5691 DMF submitted to regulatory agencies in the US is known as a USDMF. Mcn-5691 USDMF includes data on Mcn-5691's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Mcn-5691 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Mcn-5691 suppliers with USDMF on PharmaCompass.
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