NDC 71335-2041 – Oxycodone And Acetaminophen

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

Human Prescription Drug DEA schedule CII

Product NDC71335-2041

Product details

Brand name
Oxycodone And Acetaminophen
Generic name
Oxycodone and Acetaminophen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207419
Marketed since
April 11, 2017
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Oxycodone And Acetaminophen →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2041-025 TABLET in 1 BOTTLE (71335-2041-0)May 31, 2024
71335-2041-110 TABLET in 1 BOTTLE (71335-2041-1)Mar 14, 2022
71335-2041-2120 TABLET in 1 BOTTLE (71335-2041-2)Feb 1, 2022
71335-2041-328 TABLET in 1 BOTTLE (71335-2041-3)May 31, 2024
71335-2041-412 TABLET in 1 BOTTLE (71335-2041-4)May 31, 2024
71335-2041-540 TABLET in 1 BOTTLE (71335-2041-5)Mar 16, 2022
71335-2041-630 TABLET in 1 BOTTLE (71335-2041-6)Feb 18, 2022
71335-2041-790 TABLET in 1 BOTTLE (71335-2041-7)Feb 10, 2022
71335-2041-860 TABLET in 1 BOTTLE (71335-2041-8)May 9, 2022
71335-2041-984 TABLET in 1 BOTTLE (71335-2041-9)May 31, 2024

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