NDC 71335-1036 – Oxycodone and Acetaminophen

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

Human Prescription Drug DEA schedule CII

Product NDC71335-1036

Product details

Brand name
Oxycodone and Acetaminophen
Generic name
Oxycodone and Acetaminophen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA201972
Marketed since
July 15, 2013
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
71335-1036-130 TABLET in 1 BOTTLE (71335-1036-1)Jan 7, 2019
71335-1036-2120 TABLET in 1 BOTTLE (71335-1036-2)Aug 9, 2024
71335-1036-390 TABLET in 1 BOTTLE (71335-1036-3)Dec 24, 2018
71335-1036-428 TABLET in 1 BOTTLE (71335-1036-4)Aug 9, 2024
71335-1036-560 TABLET in 1 BOTTLE (71335-1036-5)Dec 24, 2018
71335-1036-620 TABLET in 1 BOTTLE (71335-1036-6)Aug 9, 2024
71335-1036-745 TABLET in 1 BOTTLE (71335-1036-7)Aug 9, 2024
71335-1036-875 TABLET in 1 BOTTLE (71335-1036-8)Aug 9, 2024
71335-1036-9100 TABLET in 1 BOTTLE (71335-1036-9)Aug 9, 2024

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