01 1M/s Centaur Pharmaceuticals Pvt Ltd
02 2M/sGlobal Calcium Pvt Ltd
01 1Flupentixol Dihydrochloride BP/EP
02 1Flupentixol Dihydrochloride Ph. Eur
03 1Flupentixol hydrochloride BP
01 2WC-0104
02 1WC-0107
01 3India
Flupentixol Dihydrochloride BP/EP
Date of Issue : 2022-06-08
Valid Till : 2025-06-25
Written Confirmation Number : WC-0107
Address of the Firm : Plot No. 75/76, 76/1 & 74, Chikhloli MIDC, Ambernath (West), Thane- 421501, Maha...
Date of Issue : 2022-06-17
Valid Till : 2025-07-07
Written Confirmation Number : WC-0104
Address of the Firm : 125 & 126, Sipcot Industrial Complex, Hosur 635126, Tamil Nadu
Flupentixol Dihydrochloride Ph. Eur
Date of Issue : 2022-06-17
Valid Till : 2025-07-07
Written Confirmation Number : WC-0104
Address of the Firm : 125 & 126, Sipcot Industrial Complex, Hosur 635126, Tamil Nadu
95
PharmaCompass offers a list of Flupentixol Dihydrochloride 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 Flupentixol Dihydrochloride manufacturer or Flupentixol Dihydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Flupentixol Dihydrochloride manufacturer or Flupentixol Dihydrochloride supplier.
PharmaCompass also assists you with knowing the Flupentixol Dihydrochloride API Price utilized in the formulation of products. Flupentixol Dihydrochloride API Price is not always fixed or binding as the Flupentixol Dihydrochloride Price is obtained through a variety of data sources. The Flupentixol Dihydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 2413-38-9 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 2413-38-9, including repackagers and relabelers. The FDA regulates 2413-38-9 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 2413-38-9 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 2413-38-9 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 2413-38-9 supplier is an individual or a company that provides 2413-38-9 active pharmaceutical ingredient (API) or 2413-38-9 finished formulations upon request. The 2413-38-9 suppliers may include 2413-38-9 API manufacturers, exporters, distributors and traders.
click here to find a list of 2413-38-9 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 2413-38-9 written confirmation (2413-38-9 WC) is an official document issued by a regulatory agency to a 2413-38-9 manufacturer, verifying that the manufacturing facility of a 2413-38-9 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 2413-38-9 APIs or 2413-38-9 finished pharmaceutical products to another nation, regulatory agencies frequently require a 2413-38-9 WC (written confirmation) as part of the regulatory process.
click here to find a list of 2413-38-9 suppliers with Written Confirmation (WC) on PharmaCompass.
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