01 1Fagron Inc
02 1LETCO MEDICAL, LLC
03 1Medisca Inc.
04 1Pharma Source Direct, Inc.
05 2Siegfried USA, LLC
06 3SpecGx LLC
07 1Spectrum Laboratory Products, Inc.
08 1VistaPharm, LLC
01 2Methadone HCl
02 1Methadone Hcl
03 8Methadone Hydrochloride
01 1India
02 3Ireland
03 1Netherlands
04 2Switzerland
05 4U.S.A
NDC Package Code : 51552-0728
Start Marketing Date : 1998-04-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 62991-1408
Start Marketing Date : 2009-12-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0406-1510
Start Marketing Date : 2012-04-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0406-8887
Start Marketing Date : 2014-06-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-9383
Start Marketing Date : 2014-06-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0104
Start Marketing Date : 2014-08-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0792-0359
Start Marketing Date : 1986-03-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0792-0360
Start Marketing Date : 2015-12-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-4553
Start Marketing Date : 2001-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66689-681
Start Marketing Date : 2009-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Methadone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methadone Hydrochloride, including repackagers and relabelers. The FDA regulates Methadone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methadone Hydrochloride 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 Methadone Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methadone Hydrochloride supplier is an individual or a company that provides Methadone Hydrochloride active pharmaceutical ingredient (API) or Methadone Hydrochloride finished formulations upon request. The Methadone Hydrochloride suppliers may include Methadone Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Methadone Hydrochloride 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 Methadone Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Methadone Hydrochloride 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 Methadone Hydrochloride 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 Methadone Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Methadone Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Methadone Hydrochloride suppliers with NDC on PharmaCompass.
We have 8 companies offering Methadone Hydrochloride
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