Home > National Drug Code (NDC) > Oxycodone Hydrochloride

Oxycodone Hydrochloride - 55289-511-60 - (Oxycodone Hydrochloride)

Alphabetical Index


Drug Information of Oxycodone Hydrochloride

Product NDC: 55289-511
Proprietary Name: Oxycodone Hydrochloride
Non Proprietary Name: Oxycodone Hydrochloride
Active Ingredient(s): 30    mg/1 & nbsp;   Oxycodone Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Oxycodone Hydrochloride

Product NDC: 55289-511
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077712
Marketing Category: ANDA
Start Marketing Date: 20070131

Package Information of Oxycodone Hydrochloride

Package NDC: 55289-511-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (55289-511-60)

NDC Information of Oxycodone Hydrochloride

NDC Code 55289-511-60
Proprietary Name Oxycodone Hydrochloride
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (55289-511-60)
Product NDC 55289-511
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070131
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name OXYCODONE HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Oxycodone Hydrochloride


General Information