01 1Ash Stevens LLC
01 1Mobocertinib
01 1U.S.A
NDC Package Code : 48957-0104
Start Marketing Date : 2021-09-15
End Marketing Date : 2026-09-30
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Mobocertinib Succinate 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 Mobocertinib Succinate manufacturer or Mobocertinib Succinate supplier for your needs.
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A Mobocertinib Succinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mobocertinib Succinate, including repackagers and relabelers. The FDA regulates Mobocertinib Succinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mobocertinib Succinate 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 Mobocertinib Succinate supplier is an individual or a company that provides Mobocertinib Succinate active pharmaceutical ingredient (API) or Mobocertinib Succinate finished formulations upon request. The Mobocertinib Succinate suppliers may include Mobocertinib Succinate 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 Mobocertinib Succinate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Mobocertinib Succinate 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 Mobocertinib Succinate 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 Mobocertinib Succinate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Mobocertinib Succinate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Mobocertinib Succinate suppliers with NDC on PharmaCompass.
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