Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
01 2CENTRIENT PHARMACEUTICALS SPAIN S.A.
02 1ACS Dobfar S.p.A
03 1Aurobindo Pharma Limited
01 1Cefadroxil
02 3Cefadroxil Monohydrate
01 1India
02 1Italy
03 2Netherlands
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
NDC Package Code : 61303-111
Start Marketing Date : 2007-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
NDC Package Code : 61303-715
Start Marketing Date : 2007-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52946-0903
Start Marketing Date : 2009-12-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-359
Start Marketing Date : 2024-01-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
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A Duracef manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Duracef, including repackagers and relabelers. The FDA regulates Duracef manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Duracef 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 Duracef supplier is an individual or a company that provides Duracef active pharmaceutical ingredient (API) or Duracef finished formulations upon request. The Duracef suppliers may include Duracef 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 Duracef as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Duracef 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 Duracef 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.
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