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METHADONE HYDROCHLORIDE - 35356-834-90 - (METHADONE HYDROCHLORIDE)

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Drug Information of METHADONE HYDROCHLORIDE

Product NDC: 35356-834
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: 35356-834
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA006134
Marketing Category: NDA
Start Marketing Date: 19470813

Package Information of METHADONE HYDROCHLORIDE

Package NDC: 35356-834-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (35356-834-90)

NDC Information of METHADONE HYDROCHLORIDE

NDC Code 35356-834-90
Proprietary Name METHADONE HYDROCHLORIDE
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (35356-834-90)
Product NDC 35356-834
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METHADONE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19470813
Marketing Category Name NDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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


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