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01 1M/s Alchymars ICM SM PVt ltd
02 1M/s Dishman Carbogen Amcis Limiteds
03 1M/sAlchymars ICM SM Pvt Ltd
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01 1Thioridazine Hydrochloride Ph.Eur./USP
02 2Thioridazine Hydrochloride USP
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01 1WC-0135
02 1WC-0348
03 1WC-348
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01 3India
Thioridazine Hydrochloride USP
Date of Issue : 2023-01-27
Valid Till : 2024-12-22
Written Confirmation Number : WC-0348
Address of the Firm : No.A-14,SIDCO Pharmaceutical Complex, Alanthur-603110, Thiruporur, Kancheepuram ...
Thioridazine Hydrochloride USP
Date of Issue : 2020-06-25
Valid Till : 2024-12-22
Written Confirmation Number : WC-348
Address of the Firm : M/s.Alchymars ICMSMPvtLtd, 27JAN|No.A-14,SIDCOPharmaceutical Complex, Alanthur-6...
Thioridazine Hydrochloride Ph.Eur./USP
Date of Issue : 2022-09-30
Valid Till : 2025-06-30
Written Confirmation Number : WC-0135
Address of the Firm : Survey No.47,48 Paiki sub Plot No.1, Village Lodariyal, Tal -Sanand, Dist -Ahmed...
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PharmaCompass offers a list of Thioridazine 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 Thioridazine Hydrochloride manufacturer or Thioridazine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Thioridazine Hydrochloride manufacturer or Thioridazine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Thioridazine Hydrochloride API Price utilized in the formulation of products. Thioridazine Hydrochloride API Price is not always fixed or binding as the Thioridazine Hydrochloride Price is obtained through a variety of data sources. The Thioridazine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Melleril (tablet) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Melleril (tablet), including repackagers and relabelers. The FDA regulates Melleril (tablet) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Melleril (tablet) 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 Melleril (tablet) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Melleril (tablet) supplier is an individual or a company that provides Melleril (tablet) active pharmaceutical ingredient (API) or Melleril (tablet) finished formulations upon request. The Melleril (tablet) suppliers may include Melleril (tablet) API manufacturers, exporters, distributors and traders.
click here to find a list of Melleril (tablet) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Melleril (tablet) written confirmation (Melleril (tablet) WC) is an official document issued by a regulatory agency to a Melleril (tablet) manufacturer, verifying that the manufacturing facility of a Melleril (tablet) active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Melleril (tablet) APIs or Melleril (tablet) finished pharmaceutical products to another nation, regulatory agencies frequently require a Melleril (tablet) WC (written confirmation) as part of the regulatory process.
click here to find a list of Melleril (tablet) suppliers with Written Confirmation (WC) on PharmaCompass.
We have 2 companies offering Melleril (tablet)
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