NDC 71335-1245 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 30 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-1245

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA091393
Marketed since
October 18, 2013
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Oxycodone Hydrochloride →

Package NDC codes (8)

Package NDCDescriptionSince
71335-1245-160 TABLET in 1 BOTTLE (71335-1245-1)Sep 20, 2019
71335-1245-290 TABLET in 1 BOTTLE (71335-1245-2)May 28, 2019
71335-1245-3120 TABLET in 1 BOTTLE (71335-1245-3)Jul 9, 2024
71335-1245-430 TABLET in 1 BOTTLE (71335-1245-4)Jul 8, 2019
71335-1245-5100 TABLET in 1 BOTTLE (71335-1245-5)Jul 9, 2024
71335-1245-640 TABLET in 1 BOTTLE (71335-1245-6)Jul 9, 2024
71335-1245-718 TABLET in 1 BOTTLE (71335-1245-7)Jul 9, 2024
71335-1245-828 TABLET in 1 BOTTLE (71335-1245-8)Jul 9, 2024

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