NDC 13107-055 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC13107-055

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone Hydrochloride
Labeler
Aurolife Pharma, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202160
Marketed since
July 12, 2012
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
13107-055-01100 TABLET in 1 BOTTLE (13107-055-01)Jul 12, 2012
13107-055-3030 TABLET in 1 BOTTLE (13107-055-30)Jul 12, 2012
13107-055-991000 TABLET in 1 BOTTLE (13107-055-99)Jul 12, 2012

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