PERCOCET - 63629-3776-2 - (oxycodone hydrochloride and acetaminophen)

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Drug Information of PERCOCET

Product NDC: 63629-3776
Proprietary Name: PERCOCET
Non Proprietary Name: oxycodone hydrochloride and acetaminophen
Active Ingredient(s): 650; 10    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: 63629-3776
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040341
Marketing Category: ANDA
Start Marketing Date: 19990730

Package Information of PERCOCET

Package NDC: 63629-3776-2
Package Description: 90 TABLET in 1 BOTTLE (63629-3776-2)

NDC Information of PERCOCET

NDC Code 63629-3776-2
Proprietary Name PERCOCET
Package Description 90 TABLET in 1 BOTTLE (63629-3776-2)
Product NDC 63629-3776
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxycodone hydrochloride and acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19990730
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Strength Number 650; 10
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of PERCOCET


General Information