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01 2Farmabios S.p.A.
02 2Sicor S.r.l.
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01 1FLUNISOLIDE
02 1FLUNISOLIDE ANHYDROUS
03 1Flunisolide Anhydrous
04 1Flunisolide Anhydrous Micronized
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01 1Germany
02 2Italy
03 1Blank
NDC Package Code : 46439-8740
Start Marketing Date : 2011-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53183-8226
Start Marketing Date : 2013-10-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53183-1226
Start Marketing Date : 2013-10-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46439-8715
Start Marketing Date : 2010-04-13
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Flunisolide 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 Flunisolide manufacturer or Flunisolide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Flunisolide manufacturer or Flunisolide supplier.
PharmaCompass also assists you with knowing the Flunisolide API Price utilized in the formulation of products. Flunisolide API Price is not always fixed or binding as the Flunisolide Price is obtained through a variety of data sources. The Flunisolide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nasalide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nasalide, including repackagers and relabelers. The FDA regulates Nasalide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nasalide 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 Nasalide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nasalide supplier is an individual or a company that provides Nasalide active pharmaceutical ingredient (API) or Nasalide finished formulations upon request. The Nasalide suppliers may include Nasalide API manufacturers, exporters, distributors and traders.
click here to find a list of Nasalide 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 Nasalide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Nasalide 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 Nasalide 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 Nasalide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Nasalide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Nasalide suppliers with NDC on PharmaCompass.