01 1ACS Dobfar S.p.A
02 1Aurobindo Pharma Limited
03 2CENTRIENT PHARMACEUTICALS SPAIN S.A.
01 1Cefadroxil
02 3Cefadroxil Monohydrate
01 1India
02 1Italy
03 2Netherlands
NDC Package Code : 52946-0903
Start Marketing Date : 2009-12-09
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-359
Start Marketing Date : 2024-01-11
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 61303-715
Start Marketing Date : 2007-06-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 61303-111
Start Marketing Date : 2007-06-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
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A CEFADROXIL/CEFADROXIL HEMIHYDRATE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CEFADROXIL/CEFADROXIL HEMIHYDRATE, including repackagers and relabelers. The FDA regulates CEFADROXIL/CEFADROXIL HEMIHYDRATE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CEFADROXIL/CEFADROXIL HEMIHYDRATE 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 CEFADROXIL/CEFADROXIL HEMIHYDRATE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A CEFADROXIL/CEFADROXIL HEMIHYDRATE supplier is an individual or a company that provides CEFADROXIL/CEFADROXIL HEMIHYDRATE active pharmaceutical ingredient (API) or CEFADROXIL/CEFADROXIL HEMIHYDRATE finished formulations upon request. The CEFADROXIL/CEFADROXIL HEMIHYDRATE suppliers may include CEFADROXIL/CEFADROXIL HEMIHYDRATE API manufacturers, exporters, distributors and traders.
click here to find a list of CEFADROXIL/CEFADROXIL HEMIHYDRATE 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 CEFADROXIL/CEFADROXIL HEMIHYDRATE as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for CEFADROXIL/CEFADROXIL HEMIHYDRATE 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 CEFADROXIL/CEFADROXIL HEMIHYDRATE 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 CEFADROXIL/CEFADROXIL HEMIHYDRATE and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a CEFADROXIL/CEFADROXIL HEMIHYDRATE NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of CEFADROXIL/CEFADROXIL HEMIHYDRATE suppliers with NDC on PharmaCompass.
We have 3 companies offering CEFADROXIL/CEFADROXIL HEMIHYDRATE
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