NDC 63629-8834 – Oxycodone And Acetaminophen

Oxycodone Hydrochloride 10 mg/1; Acetaminophen 325 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC63629-8834

Product details

Brand name
Oxycodone And Acetaminophen
Generic name
Oxycodone and Acetaminophen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207419
Marketed since
April 11, 2017
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Oxycodone And Acetaminophen →

Package NDC codes (9)

Package NDCDescriptionSince
63629-8834-130 TABLET in 1 BOTTLE (63629-8834-1)Oct 6, 2021
63629-8834-2120 TABLET in 1 BOTTLE (63629-8834-2)Oct 26, 2021
63629-8834-390 TABLET in 1 BOTTLE (63629-8834-3)Oct 7, 2021
63629-8834-428 TABLET in 1 BOTTLE (63629-8834-4)Mar 15, 2023
63629-8834-560 TABLET in 1 BOTTLE (63629-8834-5)Oct 6, 2021
63629-8834-620 TABLET in 1 BOTTLE (63629-8834-6)Mar 15, 2023
63629-8834-745 TABLET in 1 BOTTLE (63629-8834-7)Mar 15, 2023
63629-8834-875 TABLET in 1 BOTTLE (63629-8834-8)Mar 15, 2023
63629-8834-9100 TABLET in 1 BOTTLE (63629-8834-9)Mar 15, 2023

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