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METHADONE HYDROCHLORIDE - 63629-3788-4 - (METHADONE HYDROCHLORIDE)

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Drug Information of METHADONE HYDROCHLORIDE

Product NDC: 63629-3788
Proprietary Name: METHADONE HYDROCHLORIDE
Non Proprietary Name: METHADONE HYDROCHLORIDE
Active Ingredient(s): 5    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: 63629-3788
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040517
Marketing Category: ANDA
Start Marketing Date: 20090519

Package Information of METHADONE HYDROCHLORIDE

Package NDC: 63629-3788-4
Package Description: 112 TABLET in 1 BOTTLE (63629-3788-4)

NDC Information of METHADONE HYDROCHLORIDE

NDC Code 63629-3788-4
Proprietary Name METHADONE HYDROCHLORIDE
Package Description 112 TABLET in 1 BOTTLE (63629-3788-4)
Product NDC 63629-3788
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 Bryant Ranch Prepack
Substance Name METHADONE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of METHADONE HYDROCHLORIDE


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