NDC 71335-1472 – Oxycodone and Acetaminophen

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

Human Prescription Drug DEA schedule CII

Product NDC71335-1472

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
71335-1472-084 TABLET in 1 BOTTLE (71335-1472-0)Apr 3, 2024
71335-1472-1120 TABLET in 1 BOTTLE (71335-1472-1)Jun 23, 2020
71335-1472-290 TABLET in 1 BOTTLE (71335-1472-2)Mar 31, 2020
71335-1472-360 TABLET in 1 BOTTLE, PLASTIC (71335-1472-3)Feb 28, 2020
71335-1472-430 TABLET in 1 BOTTLE (71335-1472-4)Feb 14, 2020
71335-1472-5100 TABLET in 1 BOTTLE (71335-1472-5)Apr 3, 2024
71335-1472-645 TABLET in 1 BOTTLE (71335-1472-6)Jun 22, 2020
71335-1472-728 TABLET in 1 BOTTLE (71335-1472-7)Apr 3, 2024
71335-1472-8168 TABLET in 1 BOTTLE (71335-1472-8)Apr 3, 2024
71335-1472-920 TABLET in 1 BOTTLE (71335-1472-9)Apr 3, 2024

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