Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica
02 1Blank
01 1CELIPROLOL HYDROCHLORIDE
02 1CLEIPROLOL HCL
01 1Spain
02 1Blank
01 1Active
02 1Inactive
01 2Blank
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31698
Submission : 2017-05-02
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6113
Submission : 1985-12-03
Status : Inactive
Type : II
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A Selecor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Selecor, including repackagers and relabelers. The FDA regulates Selecor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Selecor API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Selecor supplier is an individual or a company that provides Selecor active pharmaceutical ingredient (API) or Selecor finished formulations upon request. The Selecor suppliers may include Selecor API manufacturers, exporters, distributors and traders.
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A Selecor DMF (Drug Master File) is a document detailing the whole manufacturing process of Selecor active pharmaceutical ingredient (API) in detail. Different forms of Selecor DMFs exist exist since differing nations have different regulations, such as Selecor USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Selecor DMF submitted to regulatory agencies in the US is known as a USDMF. Selecor USDMF includes data on Selecor's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Selecor USDMF is kept confidential to protect the manufacturer’s intellectual property.
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