01 2Aurobindo Pharma Limited
02 1Fresenius Kabi iPSUM S.r.l.
01 1OXACILLIN SODIUM
02 1Oxacillin Sodium
03 1Oxacillin for Injection
01 2India
02 1Sweden
NDC Package Code : 65862-276
Start Marketing Date : 2024-01-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-499
Start Marketing Date : 2024-01-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (49.02kg/50kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 66558-0203
Start Marketing Date : 2017-01-25
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 Oxacillin Sodium 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 Oxacillin Sodium manufacturer or Oxacillin Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxacillin Sodium manufacturer or Oxacillin Sodium supplier.
PharmaCompass also assists you with knowing the Oxacillin Sodium API Price utilized in the formulation of products. Oxacillin Sodium API Price is not always fixed or binding as the Oxacillin Sodium Price is obtained through a variety of data sources. The Oxacillin Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bristopen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bristopen, including repackagers and relabelers. The FDA regulates Bristopen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bristopen 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 Bristopen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bristopen supplier is an individual or a company that provides Bristopen active pharmaceutical ingredient (API) or Bristopen finished formulations upon request. The Bristopen suppliers may include Bristopen API manufacturers, exporters, distributors and traders.
click here to find a list of Bristopen 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 Bristopen as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Bristopen 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 Bristopen 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 Bristopen and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Bristopen NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Bristopen suppliers with NDC on PharmaCompass.
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