OPANA - 63481-617-70 - (Oxymorphone Hydrochloride)

Alphabetical Index


Drug Information of OPANA

Product NDC: 63481-617
Proprietary Name: OPANA
Non Proprietary Name: Oxymorphone Hydrochloride
Active Ingredient(s): 20    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: 63481-617
Labeler Name: Endo Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021610
Marketing Category: NDA
Start Marketing Date: 20060630

Package Information of OPANA

Package NDC: 63481-617-70
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63481-617-70)

NDC Information of OPANA

NDC Code 63481-617-70
Proprietary Name OPANA
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63481-617-70)
Product NDC 63481-617
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxymorphone Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20060630
Marketing Category Name NDA
Labeler Name Endo Pharmaceuticals
Substance Name OXYMORPHONE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of OPANA


General Information