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Oxymorphone hydrochloride - 0228-3262-50 - (Oxymorphone hydrochloride)

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Drug Information of Oxymorphone hydrochloride

Product NDC: 0228-3262
Proprietary Name: Oxymorphone hydrochloride
Non Proprietary Name: Oxymorphone hydrochloride
Active Ingredient(s): 15    mg/1 & nbsp;   Oxymorphone hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Oxymorphone hydrochloride

Product NDC: 0228-3262
Labeler Name: Actavis Elizabeth LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079046
Marketing Category: ANDA
Start Marketing Date: 20101231

Package Information of Oxymorphone hydrochloride

Package NDC: 0228-3262-50
Package Description: 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (0228-3262-50)

NDC Information of Oxymorphone hydrochloride

NDC Code 0228-3262-50
Proprietary Name Oxymorphone hydrochloride
Package Description 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (0228-3262-50)
Product NDC 0228-3262
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxymorphone hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20101231
Marketing Category Name ANDA
Labeler Name Actavis Elizabeth LLC
Substance Name OXYMORPHONE HYDROCHLORIDE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Oxymorphone hydrochloride


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