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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PharmaCompass also assists you with knowing the Celiprolol Hydrochloride API Price utilized in the formulation of products. Celiprolol Hydrochloride API Price is not always fixed or binding as the Celiprolol Hydrochloride Price is obtained through a variety of data sources. The Celiprolol Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Selectrol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Selectrol, including repackagers and relabelers. The FDA regulates Selectrol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Selectrol 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 Selectrol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Selectrol supplier is an individual or a company that provides Selectrol active pharmaceutical ingredient (API) or Selectrol finished formulations upon request. The Selectrol suppliers may include Selectrol API manufacturers, exporters, distributors and traders.
click here to find a list of Selectrol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Selectrol DMF (Drug Master File) is a document detailing the whole manufacturing process of Selectrol active pharmaceutical ingredient (API) in detail. Different forms of Selectrol DMFs exist exist since differing nations have different regulations, such as Selectrol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Selectrol DMF submitted to regulatory agencies in the US is known as a USDMF. Selectrol USDMF includes data on Selectrol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Selectrol USDMF is kept confidential to protect the manufacturer’s intellectual property.
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