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 Celiprolol clorhidrato manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Celiprolol clorhidrato, including repackagers and relabelers. The FDA regulates Celiprolol clorhidrato manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Celiprolol clorhidrato 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 Celiprolol clorhidrato DMF (Drug Master File) is a document detailing the whole manufacturing process of Celiprolol clorhidrato active pharmaceutical ingredient (API) in detail. Different forms of Celiprolol clorhidrato DMFs exist exist since differing nations have different regulations, such as Celiprolol clorhidrato USDMF, ASMF (EDMF), JDMF, CDMF, etc.
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