01 1Olon SpA
02 2Professional Compounding Centers of America dba PCCA
01 2PAROMOMYCIN SULFATE
02 1Paromomycin Sulfate
01 1Italy
02 2United Kingdom
NDC Package Code : 17337-0080
Start Marketing Date : 1990-08-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-4409
Start Marketing Date : 2013-06-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0106
Start Marketing Date : 2018-10-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
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PharmaCompass offers a list of Paromomycin 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 Paromomycin Sulfate manufacturer or Paromomycin Sulfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Paromomycin Sulfate manufacturer or Paromomycin Sulfate supplier.
PharmaCompass also assists you with knowing the Paromomycin Sulfate API Price utilized in the formulation of products. Paromomycin Sulfate API Price is not always fixed or binding as the Paromomycin Sulfate Price is obtained through a variety of data sources. The Paromomycin Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Humatin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Humatin, including repackagers and relabelers. The FDA regulates Humatin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Humatin 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 Humatin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Humatin supplier is an individual or a company that provides Humatin active pharmaceutical ingredient (API) or Humatin finished formulations upon request. The Humatin suppliers may include Humatin API manufacturers, exporters, distributors and traders.
click here to find a list of Humatin 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 Humatin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Humatin 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 Humatin 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 Humatin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Humatin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Humatin suppliers with NDC on PharmaCompass.
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