METHADOSE - 0406-8725-15 - (methadone hydrochloride)

Alphabetical Index


Drug Information of METHADOSE

Product NDC: 0406-8725
Proprietary Name: METHADOSE
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 METHADOSE

Product NDC: 0406-8725
Labeler Name: Mallinckrodt, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017116
Marketing Category: NDA
Start Marketing Date: 20100310

Package Information of METHADOSE

Package NDC: 0406-8725-15
Package Description: 15000 mL in 1 BOTTLE, PLASTIC (0406-8725-15)

NDC Information of METHADOSE

NDC Code 0406-8725-15
Proprietary Name METHADOSE
Package Description 15000 mL in 1 BOTTLE, PLASTIC (0406-8725-15)
Product NDC 0406-8725
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methadone hydrochloride
Dosage Form Name CONCENTRATE
Route Name ORAL
Start Marketing Date 20100310
Marketing Category Name NDA
Labeler Name Mallinckrodt, Inc.
Substance Name METHADONE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of METHADOSE


General Information