01 1Nira Life Sciences
01 1BENFOTIAMINE IH
01 1India
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38067
Submission : 2023-02-20
Status : Active
Type : II
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PharmaCompass offers a list of Benfotiamine 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 Benfotiamine manufacturer or Benfotiamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Benfotiamine manufacturer or Benfotiamine supplier.
PharmaCompass also assists you with knowing the Benfotiamine API Price utilized in the formulation of products. Benfotiamine API Price is not always fixed or binding as the Benfotiamine Price is obtained through a variety of data sources. The Benfotiamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Berdi manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Berdi, including repackagers and relabelers. The FDA regulates Berdi manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Berdi 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 Berdi manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Berdi supplier is an individual or a company that provides Berdi active pharmaceutical ingredient (API) or Berdi finished formulations upon request. The Berdi suppliers may include Berdi API manufacturers, exporters, distributors and traders.
click here to find a list of Berdi suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Berdi DMF (Drug Master File) is a document detailing the whole manufacturing process of Berdi active pharmaceutical ingredient (API) in detail. Different forms of Berdi DMFs exist exist since differing nations have different regulations, such as Berdi USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Berdi DMF submitted to regulatory agencies in the US is known as a USDMF. Berdi USDMF includes data on Berdi's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Berdi USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Berdi suppliers with USDMF on PharmaCompass.
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