Veranova: A CDMO that manages complexity with confidence.
01 1Veranova, L.P.
02 2Cambrex Charles City, Inc
03 1Chattem Chemicals, Inc.
04 1SpecGx LLC
01 1METHYLPHENIDATE
02 2Methylphenidate Base
03 2Methylphenidate Hydrochloride
01 1Ireland
02 4U.S.A
Veranova: A CDMO that manages complexity with confidence.
NDC Package Code : 49812-0163
Start Marketing Date : 2010-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59116-3391
Start Marketing Date : 2012-10-26
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59116-3394
Start Marketing Date : 2015-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 61960-7900
Start Marketing Date : 2003-10-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-7654
Start Marketing Date : 2013-04-01
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 Methylphenidate 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 Methylphenidate manufacturer or Methylphenidate supplier for your needs.
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A Daytrana (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Daytrana (TN), including repackagers and relabelers. The FDA regulates Daytrana (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Daytrana (TN) 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 Daytrana (TN) supplier is an individual or a company that provides Daytrana (TN) active pharmaceutical ingredient (API) or Daytrana (TN) finished formulations upon request. The Daytrana (TN) suppliers may include Daytrana (TN) 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 Daytrana (TN) as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Daytrana (TN) 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 Daytrana (TN) 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 Daytrana (TN) and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Daytrana (TN) NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Daytrana (TN) suppliers with NDC on PharmaCompass.
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