NDC 71335-9674 – Oxycodone And Acetaminophen

Oxycodone Hydrochloride 5 mg/1; Acetaminophen 325 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-9674

Product details

Brand name
Oxycodone And Acetaminophen
Generic name
Oxycodone and acetaminophen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207510
Marketed since
June 1, 2019
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (10)

Package NDCDescriptionSince
71335-9674-025 TABLET in 1 BOTTLE (71335-9674-0)Apr 13, 2026
71335-9674-110 TABLET in 1 BOTTLE (71335-9674-1)Aug 20, 2024
71335-9674-2120 TABLET in 1 BOTTLE (71335-9674-2)Apr 28, 2023
71335-9674-328 TABLET in 1 BOTTLE (71335-9674-3)Apr 13, 2026
71335-9674-412 TABLET in 1 BOTTLE (71335-9674-4)Apr 13, 2026
71335-9674-540 TABLET in 1 BOTTLE (71335-9674-5)Apr 27, 2023
71335-9674-630 TABLET in 1 BOTTLE (71335-9674-6)Jun 1, 2023
71335-9674-790 TABLET in 1 BOTTLE (71335-9674-7)Apr 13, 2026
71335-9674-860 TABLET in 1 BOTTLE (71335-9674-8)May 23, 2023
71335-9674-984 TABLET in 1 BOTTLE (71335-9674-9)Apr 13, 2026

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