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Methadone Hydrochloride - 54868-4948-2 - (Methadone Hydrochloride)

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Drug Information of Methadone Hydrochloride

Product NDC: 54868-4948
Proprietary Name: Methadone Hydrochloride
Non Proprietary Name: Methadone Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Methadone Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Methadone Hydrochloride

Product NDC: 54868-4948
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040517
Marketing Category: ANDA
Start Marketing Date: 20040107

Package Information of Methadone Hydrochloride

Package NDC: 54868-4948-2
Package Description: 120 TABLET in 1 BOTTLE (54868-4948-2)

NDC Information of Methadone Hydrochloride

NDC Code 54868-4948-2
Proprietary Name Methadone Hydrochloride
Package Description 120 TABLET in 1 BOTTLE (54868-4948-2)
Product NDC 54868-4948
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methadone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040107
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name METHADONE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Methadone Hydrochloride


General Information