Minakem is manufacturing small molecules APIs including corticosteroids
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01 2DELMAR CHEMICALS INC
02 1Emcure Pharmaceuticals Limited
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01 2PENTAMIDINE ISETHIONATE
02 1Pentamidine Isethionate
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01 2Canada
02 1India
NDC Package Code : 11712-788
Start Marketing Date : 1986-07-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 11712-790
Start Marketing Date : 1986-07-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14593-930
Start Marketing Date : 2022-02-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (15kg/15kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Pentamidine Isethionate 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 Pentamidine Isethionate manufacturer or Pentamidine Isethionate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pentamidine Isethionate manufacturer or Pentamidine Isethionate supplier.
PharmaCompass also assists you with knowing the Pentamidine Isethionate API Price utilized in the formulation of products. Pentamidine Isethionate API Price is not always fixed or binding as the Pentamidine Isethionate Price is obtained through a variety of data sources. The Pentamidine Isethionate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A NebuPent manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NebuPent, including repackagers and relabelers. The FDA regulates NebuPent manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NebuPent 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 NebuPent manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A NebuPent supplier is an individual or a company that provides NebuPent active pharmaceutical ingredient (API) or NebuPent finished formulations upon request. The NebuPent suppliers may include NebuPent API manufacturers, exporters, distributors and traders.
click here to find a list of NebuPent 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 NebuPent as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for NebuPent 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 NebuPent 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 NebuPent and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a NebuPent NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of NebuPent suppliers with NDC on PharmaCompass.
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