01 1B.V. Katwijk Chemie
02 1Professional Compounding Centers of America dba PCCA
01 2ETHOSUXIMIDE
01 1Netherlands
02 1United Kingdom
NDC Package Code : 17349-0006
Start Marketing Date : 1996-02-27
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-3436
Start Marketing Date : 2013-06-25
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 Ethosuximide 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 Ethosuximide manufacturer or Ethosuximide supplier for your needs.
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A Epileo Petit MAL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Epileo Petit MAL, including repackagers and relabelers. The FDA regulates Epileo Petit MAL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Epileo Petit MAL API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Epileo Petit MAL supplier is an individual or a company that provides Epileo Petit MAL active pharmaceutical ingredient (API) or Epileo Petit MAL finished formulations upon request. The Epileo Petit MAL suppliers may include Epileo Petit MAL API manufacturers, exporters, distributors and traders.
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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 Epileo Petit MAL as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Epileo Petit MAL 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 Epileo Petit MAL 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 Epileo Petit MAL and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Epileo Petit MAL NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Epileo Petit MAL suppliers with NDC on PharmaCompass.
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