Veranova: A CDMO that manages complexity with confidence.
01 1Veranova, L.P.
02 1American Pacific Corporation
03 2Chattem Chemicals, Inc.
04 1Curia Missouri Inc.
05 1Curia New York, Inc.
06 1S&B Pharma LLC dba Norac Pharma
07 1Siegfried USA, LLC
08 1SpecGx LLC
01 1DEXMETHYLPHENIDATE HYDROCHLORIDE
02 1Dexmethylphenidate HCl
03 3Dexmethylphenidate Hydrochloride
04 1d-Methylphenidate Base
05 1d-Methylphenidate Hydrochloride
06 1dex-Methylphenidate Hydrochloride
07 1dexmethylphenidate hydrochloride
01 1Ireland
02 1Switzerland
03 7U.S.A
Veranova: A CDMO that manages complexity with confidence.
DEXMETHYLPHENIDATE HYDROCHLORIDE
NDC Package Code : 49812-0076
Start Marketing Date : 2019-09-12
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
DEXMETHYLPHENIDATE HYDROCHLORIDE
NDC Package Code : 50683-0428
Start Marketing Date : 2017-09-04
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 61960-1724
Start Marketing Date : 2014-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DEXMETHYLPHENIDATE HYDROCHLORIDE
NDC Package Code : 61960-6900
Start Marketing Date : 2009-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DEXMETHYLPHENIDATE HYDROCHLORIDE
NDC Package Code : 65392-3418
Start Marketing Date : 2012-06-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DEXMETHYLPHENIDATE HYDROCHLORIDE
NDC Package Code : 17180-1725
Start Marketing Date : 2012-06-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DEXMETHYLPHENIDATE HYDROCHLORIDE
NDC Package Code : 0406-1039
Start Marketing Date : 2016-08-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DEXMETHYLPHENIDATE HYDROCHLORIDE
NDC Package Code : 53834-201
Start Marketing Date : 2019-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
DEXMETHYLPHENIDATE HYDROCHLORIDE
NDC Package Code : 0792-0619
Start Marketing Date : 1998-09-21
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 Dexmethylphenidate 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 Dexmethylphenidate manufacturer or Dexmethylphenidate supplier for your needs.
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PharmaCompass also assists you with knowing the Dexmethylphenidate API Price utilized in the formulation of products. Dexmethylphenidate API Price is not always fixed or binding as the Dexmethylphenidate Price is obtained through a variety of data sources. The Dexmethylphenidate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Focalin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Focalin, including repackagers and relabelers. The FDA regulates Focalin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Focalin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Focalin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Focalin supplier is an individual or a company that provides Focalin active pharmaceutical ingredient (API) or Focalin finished formulations upon request. The Focalin suppliers may include Focalin API manufacturers, exporters, distributors and traders.
click here to find a list of Focalin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 Focalin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Focalin 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 Focalin 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 Focalin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Focalin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Focalin suppliers with NDC on PharmaCompass.
We have 7 companies offering Focalin
Get in contact with the supplier of your choice:
