Home > National Drug Code (NDC) > OXYCODONE AND ACETAMINOPHEN

OXYCODONE AND ACETAMINOPHEN - 63629-4068-8 - (OXYCODONE AND ACETAMINOPHEN)

Alphabetical Index


Drug Information of OXYCODONE AND ACETAMINOPHEN

Product NDC: 63629-4068
Proprietary Name: OXYCODONE AND ACETAMINOPHEN
Non Proprietary Name: OXYCODONE AND ACETAMINOPHEN
Active Ingredient(s): 325; 7.5    mg/1; mg/1 & nbsp;   OXYCODONE AND ACETAMINOPHEN
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of OXYCODONE AND ACETAMINOPHEN

Product NDC: 63629-4068
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040535
Marketing Category: ANDA
Start Marketing Date: 20090904

Package Information of OXYCODONE AND ACETAMINOPHEN

Package NDC: 63629-4068-8
Package Description: 168 TABLET in 1 BOTTLE (63629-4068-8)

NDC Information of OXYCODONE AND ACETAMINOPHEN

NDC Code 63629-4068-8
Proprietary Name OXYCODONE AND ACETAMINOPHEN
Package Description 168 TABLET in 1 BOTTLE (63629-4068-8)
Product NDC 63629-4068
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name OXYCODONE AND ACETAMINOPHEN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090904
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Strength Number 325; 7.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of OXYCODONE AND ACETAMINOPHEN


General Information