Moehs Group, a reference company in the production of pharmaceutical active ingredients.
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01 1Moehs Iberica
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01 1CELIPROLOL HYDROCHLORIDE
02 1CLEIPROLOL HCL
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01 1Spain
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01 1Active
02 1Inactive
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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 offers a list of Celiprolol Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Celiprolol Hydrochloride manufacturer or Celiprolol Hydrochloride supplier for your needs.
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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 3-(3-Acetil-4-(3-tert-butilamino-2-hidroxipropoxi)fenil)-1,1-dietilurea HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 3-(3-Acetil-4-(3-tert-butilamino-2-hidroxipropoxi)fenil)-1,1-dietilurea HCl, including repackagers and relabelers. The FDA regulates 3-(3-Acetil-4-(3-tert-butilamino-2-hidroxipropoxi)fenil)-1,1-dietilurea HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 3-(3-Acetil-4-(3-tert-butilamino-2-hidroxipropoxi)fenil)-1,1-dietilurea HCl 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 3-(3-Acetil-4-(3-tert-butilamino-2-hidroxipropoxi)fenil)-1,1-dietilurea HCl supplier is an individual or a company that provides 3-(3-Acetil-4-(3-tert-butilamino-2-hidroxipropoxi)fenil)-1,1-dietilurea HCl active pharmaceutical ingredient (API) or 3-(3-Acetil-4-(3-tert-butilamino-2-hidroxipropoxi)fenil)-1,1-dietilurea HCl finished formulations upon request. The 3-(3-Acetil-4-(3-tert-butilamino-2-hidroxipropoxi)fenil)-1,1-dietilurea HCl suppliers may include 3-(3-Acetil-4-(3-tert-butilamino-2-hidroxipropoxi)fenil)-1,1-dietilurea HCl API manufacturers, exporters, distributors and traders.
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A 3-(3-Acetil-4-(3-tert-butilamino-2-hidroxipropoxi)fenil)-1,1-dietilurea HCl DMF (Drug Master File) is a document detailing the whole manufacturing process of 3-(3-Acetil-4-(3-tert-butilamino-2-hidroxipropoxi)fenil)-1,1-dietilurea HCl active pharmaceutical ingredient (API) in detail. Different forms of 3-(3-Acetil-4-(3-tert-butilamino-2-hidroxipropoxi)fenil)-1,1-dietilurea HCl DMFs exist exist since differing nations have different regulations, such as 3-(3-Acetil-4-(3-tert-butilamino-2-hidroxipropoxi)fenil)-1,1-dietilurea HCl USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 3-(3-Acetil-4-(3-tert-butilamino-2-hidroxipropoxi)fenil)-1,1-dietilurea HCl DMF submitted to regulatory agencies in the US is known as a USDMF. 3-(3-Acetil-4-(3-tert-butilamino-2-hidroxipropoxi)fenil)-1,1-dietilurea HCl USDMF includes data on 3-(3-Acetil-4-(3-tert-butilamino-2-hidroxipropoxi)fenil)-1,1-dietilurea HCl's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 3-(3-Acetil-4-(3-tert-butilamino-2-hidroxipropoxi)fenil)-1,1-dietilurea HCl USDMF is kept confidential to protect the manufacturer’s intellectual property.
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