PERCOCET - 54868-0510-3 - (oxycodone hydrochloride and acetaminophen)

Alphabetical Index


Drug Information of PERCOCET

Product NDC: 54868-0510
Proprietary Name: PERCOCET
Non Proprietary Name: oxycodone hydrochloride and acetaminophen
Active Ingredient(s): 325; 5    mg/1; mg/1 & nbsp;   oxycodone hydrochloride and acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of PERCOCET

Product NDC: 54868-0510
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040330
Marketing Category: ANDA
Start Marketing Date: 20000313

Package Information of PERCOCET

Package NDC: 54868-0510-3
Package Description: 10 TABLET in 1 BOTTLE, PLASTIC (54868-0510-3)

NDC Information of PERCOCET

NDC Code 54868-0510-3
Proprietary Name PERCOCET
Package Description 10 TABLET in 1 BOTTLE, PLASTIC (54868-0510-3)
Product NDC 54868-0510
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxycodone hydrochloride and acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000313
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Strength Number 325; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of PERCOCET


General Information