Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
01 1Chunghwa Chemical Synthesis & Biotech. Ltd
02 1Angelini Pharma Italia Aziende Chimiche Riunite Angelini Francesco A.C.R.A.F. Spa
03 1Hetero Drugs Limited
04 1Raks Pharma Pvt. Limited
05 1Syn-Tech Chem. & Pharm. Co., Ltd.
06 1Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd.
01 1METAXALONE
02 5Metaxalone
01 1China
02 2India
03 1Italy
04 2Taiwan
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
NDC Package Code : 52076-6231
Start Marketing Date : 2018-01-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50056-1999
Start Marketing Date : 2000-10-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65977-0089
Start Marketing Date : 2002-08-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 47621-020
Start Marketing Date : 2013-06-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54871-1087
Start Marketing Date : 2004-02-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12666-0012
Start Marketing Date : 2010-03-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Metaxalone 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 Metaxalone manufacturer or Metaxalone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Metaxalone manufacturer or Metaxalone supplier.
PharmaCompass also assists you with knowing the Metaxalone API Price utilized in the formulation of products. Metaxalone API Price is not always fixed or binding as the Metaxalone Price is obtained through a variety of data sources. The Metaxalone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A FS-3218 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of FS-3218, including repackagers and relabelers. The FDA regulates FS-3218 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. FS-3218 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 FS-3218 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A FS-3218 supplier is an individual or a company that provides FS-3218 active pharmaceutical ingredient (API) or FS-3218 finished formulations upon request. The FS-3218 suppliers may include FS-3218 API manufacturers, exporters, distributors and traders.
click here to find a list of FS-3218 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing FS-3218 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for FS-3218 API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture FS-3218 as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain FS-3218 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a FS-3218 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of FS-3218 suppliers with NDC on PharmaCompass.
We have 6 companies offering FS-3218
Get in contact with the supplier of your choice:
