Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
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01 1Biophore India Pharmaceuticals Pvt Ltd
02 1Nuray Chemicals Private Limited
03 1Cipla
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01 2ALOSETRON HYDROCHLORIDE
02 1ALOSETRON HYDROCHLORIDE USP
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01 3India
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01 3Active
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01 3Complete
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : Complete
Rev. Date : 2014-02-28
Pay. Date : 2013-09-25
DMF Number : 27470
Submission : 2013-09-23
Status : Active
Type : II
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
GDUFA
DMF Review : Complete
Rev. Date : 2013-10-19
Pay. Date : 2013-09-12
DMF Number : 27378
Submission : 2013-09-16
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-09-04
Pay. Date : 2015-08-21
DMF Number : 22125
Submission : 2009-08-19
Status : Active
Type : II
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PharmaCompass offers a list of Alosetron 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 Alosetron Hydrochloride manufacturer or Alosetron Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Alosetron Hydrochloride manufacturer or Alosetron Hydrochloride supplier.
PharmaCompass also assists you with knowing the Alosetron Hydrochloride API Price utilized in the formulation of products. Alosetron Hydrochloride API Price is not always fixed or binding as the Alosetron Hydrochloride Price is obtained through a variety of data sources. The Alosetron Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CS-0642 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CS-0642, including repackagers and relabelers. The FDA regulates CS-0642 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CS-0642 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 CS-0642 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CS-0642 supplier is an individual or a company that provides CS-0642 active pharmaceutical ingredient (API) or CS-0642 finished formulations upon request. The CS-0642 suppliers may include CS-0642 API manufacturers, exporters, distributors and traders.
click here to find a list of CS-0642 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CS-0642 DMF (Drug Master File) is a document detailing the whole manufacturing process of CS-0642 active pharmaceutical ingredient (API) in detail. Different forms of CS-0642 DMFs exist exist since differing nations have different regulations, such as CS-0642 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A CS-0642 DMF submitted to regulatory agencies in the US is known as a USDMF. CS-0642 USDMF includes data on CS-0642's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The CS-0642 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of CS-0642 suppliers with USDMF on PharmaCompass.
We have 3 companies offering CS-0642
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