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Methadone Hydrochloride - 66689-695-30 - (Methadone Hydrochloride)

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Drug Information of Methadone Hydrochloride

Product NDC: 66689-695
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: 66689-695
Labeler Name: VistaPharm Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040088
Marketing Category: ANDA
Start Marketing Date: 20111201

Package Information of Methadone Hydrochloride

Package NDC: 66689-695-30
Package Description: 30 mL in 1 BOTTLE, DROPPER (66689-695-30)

NDC Information of Methadone Hydrochloride

NDC Code 66689-695-30
Proprietary Name Methadone Hydrochloride
Package Description 30 mL in 1 BOTTLE, DROPPER (66689-695-30)
Product NDC 66689-695
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methadone Hydrochloride
Dosage Form Name CONCENTRATE
Route Name ORAL
Start Marketing Date 20111201
Marketing Category Name ANDA
Labeler Name VistaPharm 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


General Information