01 1Maithri Drugs Private Limited
01 1CARBIMAZOLE
01 1Blank
NDC Package Code : 70600-079
Start Marketing Date : 2021-03-19
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Carbimazole 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 Carbimazole manufacturer or Carbimazole supplier for your needs.
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A Neo Tomizol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neo Tomizol, including repackagers and relabelers. The FDA regulates Neo Tomizol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neo Tomizol 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 Neo Tomizol supplier is an individual or a company that provides Neo Tomizol active pharmaceutical ingredient (API) or Neo Tomizol finished formulations upon request. The Neo Tomizol suppliers may include Neo Tomizol 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 Neo Tomizol as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Neo Tomizol 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 Neo Tomizol 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 Neo Tomizol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Neo Tomizol NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Neo Tomizol suppliers with NDC on PharmaCompass.
