NDC 72189-398

Percocet

Oxycodone/apap

Percocet is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Direct_rx. The primary component is Acetaminophen; Oxycodone Hydrochloride.

Product ID72189-398_ee14972b-653b-7f56-e053-2a95a90ad1be
NDC72189-398
Product TypeHuman Prescription Drug
Proprietary NamePercocet
Generic NameOxycodone/apap
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2022-11-22
Marketing CategoryANDA /
Application NumberANDA201278
Labeler NameDirect_Rx
Substance NameACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Active Ingredient Strength325 mg/1; mg/1
Pharm ClassesFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA ScheduleCII
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 72189-398-30

30 TABLET in 1 BOTTLE (72189-398-30)
Marketing Start Date2022-11-22
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Percocet" or generic name "Oxycodone/apap"

NDCBrand NameGeneric Name
63481-623PERCOCEToxycodone hydrochloride and acetaminophen
63481-627PERCOCEToxycodone hydrochloride and acetaminophen
63481-628PERCOCEToxycodone hydrochloride and acetaminophen
63481-629PERCOCEToxycodone hydrochloride and acetaminophen
63629-3773PERCOCEToxycodone hydrochloride and acetaminophen
63629-3776PERCOCEToxycodone hydrochloride and acetaminophen
65084-298PERCOCEToxycodone hydrochloride and acetaminophen
72189-397PercocetOxycodone/APAP
72189-398PercocetOxycodone/APAP
61919-432OXYCODONE/APAPOXYCODONE/APAP
61919-524OXYCODONE/APAPOXYCODONE/APAP
61919-835Oxycodone/APAPOxycodone/APAP
72189-375Oxycodone/APAPOxycodone/APAP

Trademark Results [Percocet]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PERCOCET
PERCOCET
73072165 1051682 Live/Registered
ENDO LABORATORIES, INC.
1975-12-18

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