NDC 71335-1909 – Oxycodone and Acetaminophen

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

Human Prescription Drug DEA schedule CII

Product NDC71335-1909

Product details

Brand name
Oxycodone and Acetaminophen
Generic name
Oxycodone and Acetaminophen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA201278
Marketed since
August 28, 2014
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
71335-1909-121 TABLET in 1 BOTTLE, PLASTIC (71335-1909-1)May 15, 2026
71335-1909-236 TABLET in 1 BOTTLE, PLASTIC (71335-1909-2)May 15, 2026
71335-1909-320 TABLET in 1 BOTTLE, PLASTIC (71335-1909-3)May 15, 2026
71335-1909-430 TABLET in 1 BOTTLE, PLASTIC (71335-1909-4)Nov 8, 2022
71335-1909-545 TABLET in 1 BOTTLE, PLASTIC (71335-1909-5)May 15, 2026
71335-1909-660 TABLET in 1 BOTTLE, PLASTIC (71335-1909-6)May 15, 2026
71335-1909-790 TABLET in 1 BOTTLE, PLASTIC (71335-1909-7)May 15, 2026
71335-1909-8120 TABLET in 1 BOTTLE, PLASTIC (71335-1909-8)Nov 4, 2022

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