01 1Antibioticos do Brasil Ltda.
01 1Cephalothin Sodium
01 1Brazil
NDC Package Code : 10402-021
Start Marketing Date : 2011-06-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Cefalotin sodium Sterile API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Cefalotin sodium Sterile manufacturer or Cefalotin sodium Sterile supplier for your needs.
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A Cefalotina sodica manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefalotina sodica, including repackagers and relabelers. The FDA regulates Cefalotina sodica manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefalotina sodica 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 Cefalotina sodica supplier is an individual or a company that provides Cefalotina sodica active pharmaceutical ingredient (API) or Cefalotina sodica finished formulations upon request. The Cefalotina sodica suppliers may include Cefalotina sodica 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 Cefalotina sodica as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cefalotina sodica 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 Cefalotina sodica 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 Cefalotina sodica and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cefalotina sodica NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cefalotina sodica suppliers with NDC on PharmaCompass.
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