01 1Buchler GmbH
02 1PHARMAKINA S.A.
01 1QUININE HYDROCHLORIDE
02 1Quinine Hydrochloride
01 1Congo
02 1Germany
NDC Package Code : 12065-1703
Start Marketing Date : 1983-01-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 67729-000
Start Marketing Date : 1961-01-01
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 Quinine Hydrochloride 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 Quinine Hydrochloride manufacturer or Quinine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Quinine Hydrochloride manufacturer or Quinine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Quinine Hydrochloride API Price utilized in the formulation of products. Quinine Hydrochloride API Price is not always fixed or binding as the Quinine Hydrochloride Price is obtained through a variety of data sources. The Quinine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Quinbisul manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Quinbisul, including repackagers and relabelers. The FDA regulates Quinbisul manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Quinbisul 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 Quinbisul manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Quinbisul supplier is an individual or a company that provides Quinbisul active pharmaceutical ingredient (API) or Quinbisul finished formulations upon request. The Quinbisul suppliers may include Quinbisul API manufacturers, exporters, distributors and traders.
click here to find a list of Quinbisul 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 Quinbisul as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Quinbisul 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 Quinbisul 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 Quinbisul and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Quinbisul NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Quinbisul suppliers with NDC on PharmaCompass.
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