PERCOCET - 16590-618-82 - (oxycodone hydrochloride and acetaminophen)

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Drug Information of PERCOCET

Product NDC: 16590-618
Proprietary Name: PERCOCET
Non Proprietary Name: oxycodone hydrochloride and acetaminophen
Active Ingredient(s): 325; 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: 16590-618
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040434
Marketing Category: ANDA
Start Marketing Date: 20011130

Package Information of PERCOCET

Package NDC: 16590-618-82
Package Description: 180 TABLET in 1 BOTTLE (16590-618-82)

NDC Information of PERCOCET

NDC Code 16590-618-82
Proprietary Name PERCOCET
Package Description 180 TABLET in 1 BOTTLE (16590-618-82)
Product NDC 16590-618
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxycodone hydrochloride and acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20011130
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Strength Number 325; 10
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of PERCOCET


General Information