NDC 71335-9675 – Oxycodone And Acetaminophen

Oxycodone Hydrochloride 7.5 mg/1; Acetaminophen 325 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-9675

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 (8)

Package NDCDescriptionSince
71335-9675-121 TABLET in 1 BOTTLE (71335-9675-1)Apr 13, 2026
71335-9675-236 TABLET in 1 BOTTLE (71335-9675-2)Apr 13, 2026
71335-9675-320 TABLET in 1 BOTTLE (71335-9675-3)Apr 13, 2026
71335-9675-430 TABLET in 1 BOTTLE (71335-9675-4)Apr 13, 2026
71335-9675-545 TABLET in 1 BOTTLE (71335-9675-5)Apr 13, 2026
71335-9675-660 TABLET in 1 BOTTLE (71335-9675-6)Apr 13, 2026
71335-9675-790 TABLET in 1 BOTTLE (71335-9675-7)Apr 13, 2026
71335-9675-8120 TABLET in 1 BOTTLE (71335-9675-8)Apr 13, 2026

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