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01 1Aurobindo Pharma Limited
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01 1Dicloxacillin Sodium
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01 1India
NDC Package Code : 65862-278
Start Marketing Date : 2024-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Sodium Dicloxacillin 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 Sodium Dicloxacillin manufacturer or Sodium Dicloxacillin supplier for your needs.
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PharmaCompass also assists you with knowing the Sodium Dicloxacillin API Price utilized in the formulation of products. Sodium Dicloxacillin API Price is not always fixed or binding as the Sodium Dicloxacillin Price is obtained through a variety of data sources. The Sodium Dicloxacillin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Staphcillin A banyu manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Staphcillin A banyu, including repackagers and relabelers. The FDA regulates Staphcillin A banyu manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Staphcillin A banyu 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 Staphcillin A banyu supplier is an individual or a company that provides Staphcillin A banyu active pharmaceutical ingredient (API) or Staphcillin A banyu finished formulations upon request. The Staphcillin A banyu suppliers may include Staphcillin A banyu 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 Staphcillin A banyu as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Staphcillin A banyu 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 Staphcillin A banyu 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 Staphcillin A banyu and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Staphcillin A banyu NDC to their finished compounded human drug products, they may choose to do so.
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