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01 2ACS Dobfar S.p.A
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01 2Cefoxitin Sodium
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01 2Italy
NDC Package Code : 52946-0828
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 : 52946-0828
Start Marketing Date : 2009-12-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER, including repackagers and relabelers. The FDA regulates MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER 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 MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER supplier is an individual or a company that provides MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER active pharmaceutical ingredient (API) or MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER finished formulations upon request. The MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER suppliers may include MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER 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 MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER 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 MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER 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 MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER NDC to their finished compounded human drug products, they may choose to do so.
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