Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica
02 1PAION UK LTD
03 1Teva Pharmaceutical Industries
01 1REMIMAZOLAM
02 2REMIMAZOLAM BESYLATE
01 1Israel
02 1Spain
03 1United Kingdom
01 3Active
01 1Complete
02 2Blank
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36332
Submission : 2021-10-07
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32748
Submission : 2019-03-15
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2024-08-29
Pay. Date : 2024-05-01
DMF Number : 39813
Submission : 2024-05-30
Status : Active
Type : II
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PharmaCompass offers a list of Remimazolam 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 Remimazolam manufacturer or Remimazolam supplier for your needs.
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PharmaCompass also assists you with knowing the Remimazolam API Price utilized in the formulation of products. Remimazolam API Price is not always fixed or binding as the Remimazolam Price is obtained through a variety of data sources. The Remimazolam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Remimazolam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Remimazolam, including repackagers and relabelers. The FDA regulates Remimazolam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Remimazolam 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 Remimazolam supplier is an individual or a company that provides Remimazolam active pharmaceutical ingredient (API) or Remimazolam finished formulations upon request. The Remimazolam suppliers may include Remimazolam API manufacturers, exporters, distributors and traders.
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A Remimazolam DMF (Drug Master File) is a document detailing the whole manufacturing process of Remimazolam active pharmaceutical ingredient (API) in detail. Different forms of Remimazolam DMFs exist exist since differing nations have different regulations, such as Remimazolam USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Remimazolam DMF submitted to regulatory agencies in the US is known as a USDMF. Remimazolam USDMF includes data on Remimazolam's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Remimazolam USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Remimazolam suppliers with USDMF on PharmaCompass.
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