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Methadone Hydrochloride - 0054-0391-68 - (Methadone Hydrochloride)

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Drug Information of Methadone Hydrochloride

Product NDC: 0054-0391
Proprietary Name: Methadone Hydrochloride
Non Proprietary Name: Methadone Hydrochloride
Active Ingredient(s): 10    mg/mL & nbsp;   Methadone Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CONCENTRATE
Coding System: National Drug Codes(NDC)

Labeler Information of Methadone Hydrochloride

Product NDC: 0054-0391
Labeler Name: Roxane Laboratories, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089897
Marketing Category: ANDA
Start Marketing Date: 19880430

Package Information of Methadone Hydrochloride

Package NDC: 0054-0391-68
Package Description: 1000 mL in 1 BOTTLE (0054-0391-68)

NDC Information of Methadone Hydrochloride

NDC Code 0054-0391-68
Proprietary Name Methadone Hydrochloride
Package Description 1000 mL in 1 BOTTLE (0054-0391-68)
Product NDC 0054-0391
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methadone Hydrochloride
Dosage Form Name CONCENTRATE
Route Name ORAL
Start Marketing Date 19880430
Marketing Category Name ANDA
Labeler Name Roxane Laboratories, Inc
Substance Name METHADONE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Methadone Hydrochloride


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