NDC 71335-0316 – Oxycodone and Acetaminophen

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

Human Prescription Drug DEA schedule CII

Product NDC71335-0316

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
71335-0316-084 TABLET in 1 BOTTLE (71335-0316-0)Jan 17, 2012
71335-0316-1120 TABLET in 1 BOTTLE (71335-0316-1)Jan 17, 2012
71335-0316-290 TABLET in 1 BOTTLE (71335-0316-2)Jan 17, 2012
71335-0316-360 TABLET in 1 BOTTLE (71335-0316-3)Jan 17, 2012
71335-0316-430 TABLET in 1 BOTTLE (71335-0316-4)Jan 17, 2012
71335-0316-5100 TABLET in 1 BOTTLE (71335-0316-5)Jan 17, 2012
71335-0316-645 TABLET in 1 BOTTLE (71335-0316-6)Jan 17, 2012
71335-0316-728 TABLET in 1 BOTTLE (71335-0316-7)Jan 17, 2012
71335-0316-8168 TABLET in 1 BOTTLE (71335-0316-8)Jan 17, 2012
71335-0316-920 TABLET in 1 BOTTLE (71335-0316-9)Jan 17, 2012

Other Oxycodone And Acetaminophen products