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 2Aurobindo Pharma Limited
01 2Cefalexin Monohydrate
02 2Cephalexin
03 1Cephalexin Monohydrate
01 2India
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 : 61303-007
Start Marketing Date : 2009-10-28
End Marketing Date : 2024-12-31
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 : 61303-808
Start Marketing Date : 2007-12-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52946-0906
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 : 59651-230
Start Marketing Date : 2024-01-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-338
Start Marketing Date : 2024-01-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
A Cephalexin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cephalexin, including repackagers and relabelers. The FDA regulates Cephalexin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cephalexin 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 Cephalexin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cephalexin supplier is an individual or a company that provides Cephalexin active pharmaceutical ingredient (API) or Cephalexin finished formulations upon request. The Cephalexin suppliers may include Cephalexin API manufacturers, exporters, distributors and traders.
click here to find a list of Cephalexin 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 Cephalexin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cephalexin 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 Cephalexin 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 Cephalexin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cephalexin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cephalexin suppliers with NDC on PharmaCompass.
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