Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1Biophore India Pharmaceuticals Pvt Ltd
01 1ASCIMINIB HYDROCHLORIDE PREMIX-I
01 1India
01 1Active
01 1Blank
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 41393
Submission : 2025-02-28
Status : Active
Type : II
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PharmaCompass offers a list of Asciminib 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 Asciminib manufacturer or Asciminib supplier for your needs.
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PharmaCompass also assists you with knowing the Asciminib API Price utilized in the formulation of products. Asciminib API Price is not always fixed or binding as the Asciminib Price is obtained through a variety of data sources. The Asciminib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A asciminib hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of asciminib hydrochloride, including repackagers and relabelers. The FDA regulates asciminib hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. asciminib hydrochloride 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 asciminib hydrochloride supplier is an individual or a company that provides asciminib hydrochloride active pharmaceutical ingredient (API) or asciminib hydrochloride finished formulations upon request. The asciminib hydrochloride suppliers may include asciminib hydrochloride API manufacturers, exporters, distributors and traders.
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A asciminib hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of asciminib hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of asciminib hydrochloride DMFs exist exist since differing nations have different regulations, such as asciminib hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A asciminib hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. asciminib hydrochloride USDMF includes data on asciminib hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The asciminib hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
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