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Oxymorphone hydrochloride - 0115-1317-13 - (Oxymorphone hydrochloride)

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Drug Information of Oxymorphone hydrochloride

Product NDC: 0115-1317
Proprietary Name: Oxymorphone hydrochloride
Non Proprietary Name: Oxymorphone hydrochloride
Active Ingredient(s): 30    mg/1 & nbsp;   Oxymorphone hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Oxymorphone hydrochloride

Product NDC: 0115-1317
Labeler Name: Global Pharmaceuticals, Division of Impax Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079087
Marketing Category: ANDA
Start Marketing Date: 20130102

Package Information of Oxymorphone hydrochloride

Package NDC: 0115-1317-13
Package Description: 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1317-13)

NDC Information of Oxymorphone hydrochloride

NDC Code 0115-1317-13
Proprietary Name Oxymorphone hydrochloride
Package Description 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1317-13)
Product NDC 0115-1317
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxymorphone hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130102
Marketing Category Name ANDA
Labeler Name Global Pharmaceuticals, Division of Impax Laboratories, Inc.
Substance Name OXYMORPHONE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Oxymorphone hydrochloride


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