NDC 71335-2106 – Oxycodone And Acetaminophen

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

Human Prescription Drug DEA schedule CII

Product NDC71335-2106

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 (9)

Package NDCDescriptionSince
71335-2106-130 TABLET in 1 BOTTLE (71335-2106-1)Jul 5, 2022
71335-2106-2120 TABLET in 1 BOTTLE (71335-2106-2)May 31, 2024
71335-2106-390 TABLET in 1 BOTTLE (71335-2106-3)Jul 11, 2022
71335-2106-428 TABLET in 1 BOTTLE (71335-2106-4)May 31, 2024
71335-2106-560 TABLET in 1 BOTTLE (71335-2106-5)Jun 10, 2022
71335-2106-620 TABLET in 1 BOTTLE (71335-2106-6)May 31, 2024
71335-2106-745 TABLET in 1 BOTTLE (71335-2106-7)May 31, 2024
71335-2106-875 TABLET in 1 BOTTLE (71335-2106-8)May 31, 2024
71335-2106-9100 TABLET in 1 BOTTLE (71335-2106-9)May 31, 2024

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