Veranova: A CDMO that manages complexity with confidence.
01 1Veranova, L.P.
02 1Chongqing Biocare Pharmaceutical Ltd.
01 2Phytonadione
01 1U.S.A
02 1Blank
Veranova: A CDMO that manages complexity with confidence.
NDC Package Code : 49812-0232
Start Marketing Date : 2016-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 33656-0010
Start Marketing Date : 2018-10-22
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 Vitamin K1 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 Vitamin K1 manufacturer or Vitamin K1 supplier for your needs.
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A Vitamin K1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vitamin K1, including repackagers and relabelers. The FDA regulates Vitamin K1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vitamin K1 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 Vitamin K1 supplier is an individual or a company that provides Vitamin K1 active pharmaceutical ingredient (API) or Vitamin K1 finished formulations upon request. The Vitamin K1 suppliers may include Vitamin K1 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 Vitamin K1 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Vitamin K1 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 Vitamin K1 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 Vitamin K1 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Vitamin K1 NDC to their finished compounded human drug products, they may choose to do so.
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