01 1DEVATS INDIA
01 1NIMORAZOLE
01 1India
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24814
Submission : 2011-03-30
Status : Active
Type : II
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PharmaCompass offers a list of Nimorazole 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 Nimorazole manufacturer or Nimorazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nimorazole manufacturer or Nimorazole supplier.
PharmaCompass also assists you with knowing the Nimorazole API Price utilized in the formulation of products. Nimorazole API Price is not always fixed or binding as the Nimorazole Price is obtained through a variety of data sources. The Nimorazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Acterol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acterol, including repackagers and relabelers. The FDA regulates Acterol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acterol 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 Acterol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Acterol supplier is an individual or a company that provides Acterol active pharmaceutical ingredient (API) or Acterol finished formulations upon request. The Acterol suppliers may include Acterol API manufacturers, exporters, distributors and traders.
click here to find a list of Acterol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Acterol DMF (Drug Master File) is a document detailing the whole manufacturing process of Acterol active pharmaceutical ingredient (API) in detail. Different forms of Acterol DMFs exist exist since differing nations have different regulations, such as Acterol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Acterol DMF submitted to regulatory agencies in the US is known as a USDMF. Acterol USDMF includes data on Acterol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Acterol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Acterol suppliers with USDMF on PharmaCompass.
