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01 1Hunan Jiudian Pharmaceutical Co.,Ltd.
02 1ISP Sutton Laboratories
03 1SALICYLATES & CHEMICALS PRIVATE LIMITED
04 1Spectrum Laboratory Products, Inc.
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01 2ALLANTOIN
02 1Allantoin
03 1allantoin
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01 1China
02 1India
03 2U.S.A
NDC Package Code : 49574-516
Start Marketing Date : 2017-05-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51040-000
Start Marketing Date : 2012-06-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 76107-900
Start Marketing Date : 2012-11-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-0260
Start Marketing Date : 2009-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Glyoxyldiureide 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 Glyoxyldiureide manufacturer or Glyoxyldiureide supplier for your needs.
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PharmaCompass also assists you with knowing the Glyoxyldiureide API Price utilized in the formulation of products. Glyoxyldiureide API Price is not always fixed or binding as the Glyoxyldiureide Price is obtained through a variety of data sources. The Glyoxyldiureide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Allantoin, European Pharmacopoeia (EP) Reference Standard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Allantoin, European Pharmacopoeia (EP) Reference Standard, including repackagers and relabelers. The FDA regulates Allantoin, European Pharmacopoeia (EP) Reference Standard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Allantoin, European Pharmacopoeia (EP) Reference Standard 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 Allantoin, European Pharmacopoeia (EP) Reference Standard manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Allantoin, European Pharmacopoeia (EP) Reference Standard supplier is an individual or a company that provides Allantoin, European Pharmacopoeia (EP) Reference Standard active pharmaceutical ingredient (API) or Allantoin, European Pharmacopoeia (EP) Reference Standard finished formulations upon request. The Allantoin, European Pharmacopoeia (EP) Reference Standard suppliers may include Allantoin, European Pharmacopoeia (EP) Reference Standard API manufacturers, exporters, distributors and traders.
click here to find a list of Allantoin, European Pharmacopoeia (EP) Reference Standard 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 Allantoin, European Pharmacopoeia (EP) Reference Standard as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Allantoin, European Pharmacopoeia (EP) Reference Standard 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 Allantoin, European Pharmacopoeia (EP) Reference Standard 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 Allantoin, European Pharmacopoeia (EP) Reference Standard and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Allantoin, European Pharmacopoeia (EP) Reference Standard NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Allantoin, European Pharmacopoeia (EP) Reference Standard suppliers with NDC on PharmaCompass.
We have 4 companies offering Allantoin, European Pharmacopoeia (EP) Reference Standard
Get in contact with the supplier of your choice: