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METHADONE HYDROCHLORIDE - 52959-386-60 - (METHADONE HYDROCHLORIDE)

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Drug Information of METHADONE HYDROCHLORIDE

Product NDC: 52959-386
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: 52959-386
Labeler Name: H.J. Harkins Company Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040517
Marketing Category: ANDA
Start Marketing Date: 20090519

Package Information of METHADONE HYDROCHLORIDE

Package NDC: 52959-386-60
Package Description: 60 TABLET in 1 BOTTLE (52959-386-60)

NDC Information of METHADONE HYDROCHLORIDE

NDC Code 52959-386-60
Proprietary Name METHADONE HYDROCHLORIDE
Package Description 60 TABLET in 1 BOTTLE (52959-386-60)
Product NDC 52959-386
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METHADONE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090519
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company 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


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