NDC 71335-1492 – Oxycodone and Acetaminophen

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

Human Prescription Drug DEA schedule CII

Product NDC71335-1492

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 (10)

Package NDCDescriptionSince
71335-1492-025 TABLET in 1 BOTTLE (71335-1492-0)Apr 3, 2024
71335-1492-110 TABLET in 1 BOTTLE (71335-1492-1)Dec 11, 2020
71335-1492-2120 TABLET in 1 BOTTLE (71335-1492-2)Sep 21, 2020
71335-1492-328 TABLET in 1 BOTTLE (71335-1492-3)Apr 3, 2024
71335-1492-412 TABLET in 1 BOTTLE (71335-1492-4)Mar 9, 2020
71335-1492-540 TABLET in 1 BOTTLE (71335-1492-5)Mar 6, 2020
71335-1492-630 TABLET in 1 BOTTLE (71335-1492-6)Jan 21, 2020
71335-1492-790 TABLET in 1 BOTTLE (71335-1492-7)Jun 11, 2020
71335-1492-860 TABLET in 1 BOTTLE (71335-1492-8)Apr 22, 2020
71335-1492-984 TABLET in 1 BOTTLE (71335-1492-9)Apr 3, 2024

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