Drugplain

NDC 76420-362-05

Oxycodone Hydrochloride 5 mg/1

Oxycodone Hydrochloride · TABLET

No Recall History

Oxycodone Hydrochloride is a tablet containing oxycodone hydrochloride at a strength of 5 mg/1. Manufactured by Asclemed USA, Inc..

Key Facts

Brand Name
Oxycodone Hydrochloride
Generic Name
Oxycodone Hydrochloride
NDC Code (Package)
76420-362-05
NDC Code (Product)
76420-362
Manufacturer
Asclemed USA, Inc.
Strength
5 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
DEA Schedule
Schedule II (Controlled)
Application #
ANDA077712
Marketing Start
09/10/2024

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.