NDC 71335-2049 – Oxycodone And Acetaminophen

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

Human Prescription Drug DEA schedule CII

Product NDC71335-2049

Product details

Brand name
Oxycodone And Acetaminophen
Generic name
oxycodone and acetaminophen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207510
Marketed since
June 1, 2019
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
71335-2049-130 TABLET in 1 BOTTLE (71335-2049-1)Feb 28, 2022
71335-2049-2120 TABLET in 1 BOTTLE (71335-2049-2)Feb 28, 2022
71335-2049-390 TABLET in 1 BOTTLE (71335-2049-3)Feb 28, 2022
71335-2049-428 TABLET in 1 BOTTLE (71335-2049-4)Feb 28, 2022
71335-2049-560 TABLET in 1 BOTTLE (71335-2049-5)Feb 28, 2022
71335-2049-620 TABLET in 1 BOTTLE (71335-2049-6)Feb 28, 2022
71335-2049-745 TABLET in 1 BOTTLE (71335-2049-7)Feb 28, 2022
71335-2049-875 TABLET in 1 BOTTLE (71335-2049-8)Feb 28, 2022
71335-2049-9100 TABLET in 1 BOTTLE (71335-2049-9)Feb 28, 2022

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