NDC 71335-0216 – Oxycodone and Acetaminophen

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

Human Prescription Drug DEA schedule CII

Product NDC71335-0216

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
March 9, 2016
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
71335-0216-025 TABLET in 1 BOTTLE (71335-0216-0)Jul 25, 2016
71335-0216-110 TABLET in 1 BOTTLE (71335-0216-1)Jul 25, 2016
71335-0216-2120 TABLET in 1 BOTTLE (71335-0216-2)Jul 25, 2016
71335-0216-328 TABLET in 1 BOTTLE (71335-0216-3)Jul 25, 2016
71335-0216-412 TABLET in 1 BOTTLE (71335-0216-4)Jul 25, 2016
71335-0216-540 TABLET in 1 BOTTLE (71335-0216-5)Jul 25, 2016
71335-0216-630 TABLET in 1 BOTTLE (71335-0216-6)Jul 25, 2016
71335-0216-790 TABLET in 1 BOTTLE (71335-0216-7)Jul 25, 2016
71335-0216-860 TABLET in 1 BOTTLE (71335-0216-8)Jul 25, 2016
71335-0216-984 TABLET in 1 BOTTLE (71335-0216-9)Jul 25, 2016

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