OPANA - 63481-571-75 - (Oxymorphone Hydrochloride)

Alphabetical Index


Drug Information of OPANA

Product NDC: 63481-571
Proprietary Name: OPANA
Non Proprietary Name: Oxymorphone Hydrochloride
Active Ingredient(s): 30    mg/1 & nbsp;   Oxymorphone Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of OPANA

Product NDC: 63481-571
Labeler Name: Endo Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021610
Marketing Category: NDA
Start Marketing Date: 20080301

Package Information of OPANA

Package NDC: 63481-571-75
Package Description: 5 BLISTER PACK in 1 BOX, UNIT-DOSE (63481-571-75) > 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of OPANA

NDC Code 63481-571-75
Proprietary Name OPANA
Package Description 5 BLISTER PACK in 1 BOX, UNIT-DOSE (63481-571-75) > 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 63481-571
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxymorphone Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080301
Marketing Category Name NDA
Labeler Name Endo Pharmaceuticals
Substance Name OXYMORPHONE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of OPANA


General Information