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 ID: 72189-398_ee14972b-653b-7f56-e053-2a95a90ad1be
• NDC: 72189-398
• Product Type: Human Prescription Drug
• Proprietary Name: Percocet
• Generic Name: Oxycodone/apap
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2022-11-22
• Marketing Category: ANDA /
• Application Number: ANDA201278
• Labeler Name: Direct_Rx
• Substance Name: ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
• Active Ingredient Strength: 325 mg/1; mg/1
• Pharm Classes: Full Opioid Agonists [MoA], Opioid Agonist [EPC]
• DEA Schedule: CII
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 72189-398-30

30 TABLET in 1 BOTTLE (72189-398-30)

• Marketing Start Date: 2022-11-22
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

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

NDC	Brand Name	Generic Name
63481-623	PERCOCET	oxycodone hydrochloride and acetaminophen
63481-627	PERCOCET	oxycodone hydrochloride and acetaminophen
63481-628	PERCOCET	oxycodone hydrochloride and acetaminophen
63481-629	PERCOCET	oxycodone hydrochloride and acetaminophen
63629-3773	PERCOCET	oxycodone hydrochloride and acetaminophen
63629-3776	PERCOCET	oxycodone hydrochloride and acetaminophen
65084-298	PERCOCET	oxycodone hydrochloride and acetaminophen
72189-397	Percocet	Oxycodone/APAP
72189-398	Percocet	Oxycodone/APAP
61919-432	OXYCODONE/APAP	OXYCODONE/APAP
61919-524	OXYCODONE/APAP	OXYCODONE/APAP
61919-835	Oxycodone/APAP	Oxycodone/APAP
72189-375	Oxycodone/APAP	Oxycodone/APAP