OXYCONTIN - 16590-617-86 - (OXYCODONE HYDROCHLORIDE)

Alphabetical Index


Drug Information of OXYCONTIN

Product NDC: 16590-617
Proprietary Name: OXYCONTIN
Non Proprietary Name: OXYCODONE HYDROCHLORIDE
Active Ingredient(s): 80    mg/1 & nbsp;   OXYCODONE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of OXYCONTIN

Product NDC: 16590-617
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020553
Marketing Category: NDA
Start Marketing Date: 19970101

Package Information of OXYCONTIN

Package NDC: 16590-617-86
Package Description: 270 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16590-617-86)

NDC Information of OXYCONTIN

NDC Code 16590-617-86
Proprietary Name OXYCONTIN
Package Description 270 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16590-617-86)
Product NDC 16590-617
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name OXYCODONE HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19970101
Marketing Category Name NDA
Labeler Name STAT RX USA LLC
Substance Name OXYCODONE HYDROCHLORIDE
Strength Number 80
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of OXYCONTIN


General Information