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NALTREXONE HYDROCHLORIDE - 47335-326-18 - (NALTREXONE HYDROCHLORIDE)

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Drug Information of NALTREXONE HYDROCHLORIDE

Product NDC: 47335-326
Proprietary Name: NALTREXONE HYDROCHLORIDE
Non Proprietary Name: NALTREXONE HYDROCHLORIDE
Active Ingredient(s): 50    mg/1 & nbsp;   NALTREXONE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of NALTREXONE HYDROCHLORIDE

Product NDC: 47335-326
Labeler Name: Sun Pharma Global FZE
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090356
Marketing Category: ANDA
Start Marketing Date: 20120229

Package Information of NALTREXONE HYDROCHLORIDE

Package NDC: 47335-326-18
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (47335-326-18)

NDC Information of NALTREXONE HYDROCHLORIDE

NDC Code 47335-326-18
Proprietary Name NALTREXONE HYDROCHLORIDE
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (47335-326-18)
Product NDC 47335-326
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NALTREXONE HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120229
Marketing Category Name ANDA
Labeler Name Sun Pharma Global FZE
Substance Name NALTREXONE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Opioid Antagonist [EPC],Opioid Antagonists [MoA]

Complete Information of NALTREXONE HYDROCHLORIDE


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