01 1Suven Pharmaceuticals Limited
01 1Bretylium Tosylate
01 1India
NDC Package Code : 68022-7060
Start Marketing Date : 2018-12-26
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 Bretylium Tosylate 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 Bretylium Tosylate manufacturer or Bretylium Tosylate supplier for your needs.
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PharmaCompass also assists you with knowing the Bretylium Tosylate API Price utilized in the formulation of products. Bretylium Tosylate API Price is not always fixed or binding as the Bretylium Tosylate Price is obtained through a variety of data sources. The Bretylium Tosylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bretilio tosilato manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bretilio tosilato, including repackagers and relabelers. The FDA regulates Bretilio tosilato manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bretilio tosilato API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Bretilio tosilato supplier is an individual or a company that provides Bretilio tosilato active pharmaceutical ingredient (API) or Bretilio tosilato finished formulations upon request. The Bretilio tosilato suppliers may include Bretilio tosilato API manufacturers, exporters, distributors and traders.
click here to find a list of Bretilio tosilato 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 Bretilio tosilato as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Bretilio tosilato 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 Bretilio tosilato 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 Bretilio tosilato and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Bretilio tosilato NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Bretilio tosilato suppliers with NDC on PharmaCompass.
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