Opana ER - 63629-4174-1 - (OXYMORPHONE HYDROCHLORIDE)

Alphabetical Index


Drug Information of Opana ER

Product NDC: 63629-4174
Proprietary Name: Opana ER
Non Proprietary Name: OXYMORPHONE HYDROCHLORIDE
Active Ingredient(s): 20    mg/1 & nbsp;   OXYMORPHONE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Opana ER

Product NDC: 63629-4174
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021610
Marketing Category: NDA
Start Marketing Date: 20101231

Package Information of Opana ER

Package NDC: 63629-4174-1
Package Description: 60 TABLET in 1 BOTTLE (63629-4174-1)

NDC Information of Opana ER

NDC Code 63629-4174-1
Proprietary Name Opana ER
Package Description 60 TABLET in 1 BOTTLE (63629-4174-1)
Product NDC 63629-4174
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name OXYMORPHONE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101231
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
Substance Name OXYMORPHONE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Opana ER


General Information