NDC 71335-0146 – Oxycodone and Acetaminophen

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

Human Prescription Drug DEA schedule CII

Product NDC71335-0146

Product details

Brand name
Oxycodone and Acetaminophen
Generic name
Oxycodone and Acetaminophen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202677
Marketed since
January 17, 2012
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
71335-0146-0112 TABLET in 1 BOTTLE (71335-0146-0)Jan 17, 2012
71335-0146-130 TABLET in 1 BOTTLE (71335-0146-1)Jan 17, 2012
71335-0146-2120 TABLET in 1 BOTTLE (71335-0146-2)Jan 17, 2012
71335-0146-390 TABLET in 1 BOTTLE (71335-0146-3)Jan 17, 2012
71335-0146-428 TABLET in 1 BOTTLE (71335-0146-4)Jan 17, 2012
71335-0146-560 TABLET in 1 BOTTLE (71335-0146-5)Jan 17, 2012
71335-0146-620 TABLET in 1 BOTTLE (71335-0146-6)Jan 17, 2012
71335-0146-745 TABLET in 1 BOTTLE (71335-0146-7)Jan 17, 2012
71335-0146-875 TABLET in 1 BOTTLE (71335-0146-8)Jan 17, 2012
71335-0146-9100 TABLET in 1 BOTTLE (71335-0146-9)Jan 17, 2012

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