01 1Cipla Ltd.
01 1LEVALBUTEROL SULFATE
01 1India
NDC Package Code : 53104-7615
Start Marketing Date : 2016-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Levalbuterol Sulfate 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 Levalbuterol Sulfate manufacturer or Levalbuterol Sulfate supplier for your needs.
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PharmaCompass also assists you with knowing the Levalbuterol Sulfate API Price utilized in the formulation of products. Levalbuterol Sulfate API Price is not always fixed or binding as the Levalbuterol Sulfate Price is obtained through a variety of data sources. The Levalbuterol Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Levosalbutamol Sulphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levosalbutamol Sulphate, including repackagers and relabelers. The FDA regulates Levosalbutamol Sulphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levosalbutamol Sulphate 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 Levosalbutamol Sulphate supplier is an individual or a company that provides Levosalbutamol Sulphate active pharmaceutical ingredient (API) or Levosalbutamol Sulphate finished formulations upon request. The Levosalbutamol Sulphate suppliers may include Levosalbutamol Sulphate API manufacturers, exporters, distributors and traders.
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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 Levosalbutamol Sulphate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Levosalbutamol Sulphate 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 Levosalbutamol Sulphate 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 Levosalbutamol Sulphate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Levosalbutamol Sulphate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Levosalbutamol Sulphate suppliers with NDC on PharmaCompass.
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