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naltrexone hydrochloride - 0185-0039-01 - (naltrexone hydrochloride)

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Drug Information of naltrexone hydrochloride

Product NDC: 0185-0039
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: 0185-0039
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075434
Marketing Category: ANDA
Start Marketing Date: 20000308

Package Information of naltrexone hydrochloride

Package NDC: 0185-0039-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0185-0039-01)

NDC Information of naltrexone hydrochloride

NDC Code 0185-0039-01
Proprietary Name naltrexone hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0185-0039-01)
Product NDC 0185-0039
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name naltrexone hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20000308
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
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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