01 1Suven Pharmaceuticals Limited
01 1Doxofylline
01 1India
NDC Package Code : 68022-7007
Start Marketing Date : 2016-02-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
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PharmaCompass offers a list of Doxofylline 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 Doxofylline manufacturer or Doxofylline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Doxofylline manufacturer or Doxofylline supplier.
PharmaCompass also assists you with knowing the Doxofylline API Price utilized in the formulation of products. Doxofylline API Price is not always fixed or binding as the Doxofylline Price is obtained through a variety of data sources. The Doxofylline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ansimar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ansimar, including repackagers and relabelers. The FDA regulates Ansimar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ansimar 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 Ansimar manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ansimar supplier is an individual or a company that provides Ansimar active pharmaceutical ingredient (API) or Ansimar finished formulations upon request. The Ansimar suppliers may include Ansimar API manufacturers, exporters, distributors and traders.
click here to find a list of Ansimar 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 Ansimar as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ansimar 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 Ansimar 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 Ansimar and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ansimar NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ansimar suppliers with NDC on PharmaCompass.
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