NDC 76420-362-01
Oxycodone Hydrochloride 5 mg/1
Oxycodone Hydrochloride · TABLET
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)
76420-362-01- 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 HistoryView Full Drug Page
Oxycodone Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.