Home > National Drug Code (NDC) > Oxycodone Hydrochloride

Oxycodone Hydrochloride - 63629-4184-3 - (Oxycodone Hydrochloride)

Alphabetical Index


Drug Information of Oxycodone Hydrochloride

Product NDC: 63629-4184
Proprietary Name: Oxycodone Hydrochloride
Non Proprietary Name: Oxycodone Hydrochloride
Active Ingredient(s): 5    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: 63629-4184
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077712
Marketing Category: ANDA
Start Marketing Date: 20090302

Package Information of Oxycodone Hydrochloride

Package NDC: 63629-4184-3
Package Description: 90 TABLET in 1 BOTTLE (63629-4184-3)

NDC Information of Oxycodone Hydrochloride

NDC Code 63629-4184-3
Proprietary Name Oxycodone Hydrochloride
Package Description 90 TABLET in 1 BOTTLE (63629-4184-3)
Product NDC 63629-4184
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxycodone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090302
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name OXYCODONE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Oxycodone Hydrochloride


General Information