01 2Aurobindo Pharma Limited
02 2Covalent Laboratories Private Limited
03 1Olon SpA
04 1PURE AND CURE HEALTHCARE PRIVATE LIMITED
01 1CEFDINIR
02 2Cefdinir
03 1Cefdinir (Anhydrous)
04 1Cefdinir Hydrate
05 1Cefidinir
01 4India
02 1Italy
03 1Blank
NDC Package Code : 59651-947
Start Marketing Date : 2024-02-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-384
Start Marketing Date : 2024-01-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 61788-2100
Start Marketing Date : 2016-02-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 61788-2000
Start Marketing Date : 2015-04-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0302
Start Marketing Date : 2004-02-03
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82608-012
Start Marketing Date : 2022-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Cefdinir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefdinir, including repackagers and relabelers. The FDA regulates Cefdinir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefdinir 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 Cefdinir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cefdinir supplier is an individual or a company that provides Cefdinir active pharmaceutical ingredient (API) or Cefdinir finished formulations upon request. The Cefdinir suppliers may include Cefdinir API manufacturers, exporters, distributors and traders.
click here to find a list of Cefdinir 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 Cefdinir as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cefdinir 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 Cefdinir 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 Cefdinir and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cefdinir NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cefdinir suppliers with NDC on PharmaCompass.
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