01 1PCAS
02 1Erregierre SpA
03 1Medisca Inc.
04 1Olon SpA
05 1Professional Compounding Centers of America dba PCCA
01 2CICLOPIROX OLAMINE
02 2Ciclopirox Olamine
03 1Ciclopirox olamine
01 1France
02 1Italy
03 1U.S.A
04 1United Kingdom
05 1Blank
NDC Package Code : 49169-1033
Start Marketing Date : 2010-07-07
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49706-1441
Start Marketing Date : 2010-01-08
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0313
Start Marketing Date : 2014-06-06
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-3069
Start Marketing Date : 2013-06-26
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 17337-0507
Start Marketing Date : 2017-02-22
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Ciclopirox Olamine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Ciclopirox Olamine manufacturer or Ciclopirox Olamine supplier for your needs.
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A C12H17NO2.C2H7NO manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C12H17NO2.C2H7NO, including repackagers and relabelers. The FDA regulates C12H17NO2.C2H7NO manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C12H17NO2.C2H7NO 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 C12H17NO2.C2H7NO supplier is an individual or a company that provides C12H17NO2.C2H7NO active pharmaceutical ingredient (API) or C12H17NO2.C2H7NO finished formulations upon request. The C12H17NO2.C2H7NO suppliers may include C12H17NO2.C2H7NO API manufacturers, exporters, distributors and traders.
click here to find a list of C12H17NO2.C2H7NO suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 C12H17NO2.C2H7NO as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for C12H17NO2.C2H7NO 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 C12H17NO2.C2H7NO 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 C12H17NO2.C2H7NO and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a C12H17NO2.C2H7NO NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of C12H17NO2.C2H7NO suppliers with NDC on PharmaCompass.
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