01 1ACS Dobfar S.p.A
02 1ACS Dobfar SpA
03 1Aurobindo Pharma Limited
04 1Fresenius Kabi iPSUM S.r.l.
01 1NAFCILLIN SODIUM
02 2Nafcillin Sodium
03 1Nafcillin for Injection
01 1India
02 2Italy
03 1Sweden
NDC Package Code : 52946-0819
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 : 52946-0922
Start Marketing Date : 2012-08-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-500
Start Marketing Date : 2024-01-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (48kg/50kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 66558-0202
Start Marketing Date : 2011-05-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Nallpen In Plastic Container manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nallpen In Plastic Container, including repackagers and relabelers. The FDA regulates Nallpen In Plastic Container manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nallpen 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 Nallpen In Plastic Container supplier is an individual or a company that provides Nallpen In Plastic Container active pharmaceutical ingredient (API) or Nallpen In Plastic Container finished formulations upon request. The Nallpen In Plastic Container suppliers may include Nallpen 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 Nallpen In Plastic Container as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Nallpen 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 Nallpen 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 Nallpen In Plastic Container and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Nallpen In Plastic Container NDC to their finished compounded human drug products, they may choose to do so.
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