01 1Amicogen (China) Biopharm Co., Ltd
02 3Amicogen(China) Biopharm Co., Ltd
03 2Aurobindo Pharma Limited
04 1Orchid Pharma Ltd
05 1Zhejiang Apeloa Tospo Pharmaceutical Co., Ltd.
01 1Ceftiofur Crystalline Free Acid Micronized
02 3Ceftiofur Hydrochloride
03 1Ceftiofur Micronized
04 2Ceftiofur hydrochloride
05 1ceftiofur free acid sterile
01 5China
02 1Egypt
03 2India
NDC Package Code : 71411-0008
Start Marketing Date : 2022-03-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71411-0005
Start Marketing Date : 2017-06-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71411-0002
Start Marketing Date : 2017-06-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71411-0001
Start Marketing Date : 2017-06-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-314
Start Marketing Date : 2023-11-06
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-485
Start Marketing Date : 2024-01-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63785-115
Start Marketing Date : 2014-04-23
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 86185-114
Start Marketing Date : 2023-01-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A ceftiofur hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ceftiofur hydrochloride, including repackagers and relabelers. The FDA regulates ceftiofur hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ceftiofur hydrochloride 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 hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ceftiofur hydrochloride supplier is an individual or a company that provides ceftiofur hydrochloride active pharmaceutical ingredient (API) or ceftiofur hydrochloride finished formulations upon request. The ceftiofur hydrochloride suppliers may include ceftiofur hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of ceftiofur hydrochloride 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 hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for ceftiofur hydrochloride 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 hydrochloride 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 hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a ceftiofur hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of ceftiofur hydrochloride suppliers with NDC on PharmaCompass.
We have 4 companies offering ceftiofur hydrochloride
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