01 1Amicogen(China) Biopharm Co.,Ltd
02 1Aurobindo Pharma Limited
03 1Orchid Pharma Ltd
04 1Zhejiang Apeloa Tospo Pharmaceutical Co., Ltd.
01 4Ceftiofur Sodium
01 2China
02 1Egypt
03 1India
NDC Package Code : 71411-0003
Start Marketing Date : 2017-06-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59651-470
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 : 63785-105
Start Marketing Date : 2011-07-29
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 86185-108
Start Marketing Date : 2022-08-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Ceftiofur Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ceftiofur Sodium, including repackagers and relabelers. The FDA regulates Ceftiofur Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ceftiofur Sodium 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 Ceftiofur Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ceftiofur Sodium supplier is an individual or a company that provides Ceftiofur Sodium active pharmaceutical ingredient (API) or Ceftiofur Sodium finished formulations upon request. The Ceftiofur Sodium suppliers may include Ceftiofur Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Ceftiofur Sodium 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 Ceftiofur Sodium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ceftiofur Sodium 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 Ceftiofur Sodium 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 Ceftiofur Sodium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ceftiofur Sodium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ceftiofur Sodium suppliers with NDC on PharmaCompass.
We have 4 companies offering Ceftiofur Sodium
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