OxyContin 80 mg/1
oxycodone hydrochloride · TABLET, FILM COATED, EXTENDED RELEASE · Knoa Pharma LLC
OxyContin is a tablet, film coated, extended release containing oxycodone hydrochloride at 80 mg/1, taken oral. Manufactured by Knoa Pharma LLC.
Key Facts
- Brand Name
- OxyContin
- Generic Name
- oxycodone hydrochloride
- NDC Code (Product)
59011-480- Manufacturer
- Knoa Pharma LLC
- Strength
- 80 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- DEA Schedule
- Schedule II (Controlled)
- Application #
- NDA022272
- Marketing Start
- 08/08/2010
Recall History
No Recall HistoryFrequently Asked Questions
What is OxyContin used for?
OxyContin contains oxycodone hydrochloride. It is a tablet, film coated, extended release taken oral. Consult your doctor for specific uses.
Is OxyContin a controlled substance?
Yes, OxyContin is classified as CII under the DEA Controlled Substances Act.
What is the generic name for OxyContin?
The generic name for OxyContin is oxycodone hydrochloride. There are 12 other brand versions of oxycodone hydrochloride.
What is the NDC code for OxyContin 80 mg/1?
The NDC (National Drug Code) for OxyContin 80 mg/1 is 59011-480, listed by Knoa Pharma LLC.
Other Oxycodone Brands
See all →- Oxycodone Hydrochloride15 mg/176420-364
- Oxycodone hydrochloride30 mg/176420-768
- RoxyBond30 mg/181140-103
- Roxicodone30 mg/123635-582
- Oxycodone Hydrochloride15 mg/142806-007
- Oxycodone Hydrochloride5 mg/142858-001
- Oxycodone Hydrochloride10 mg/143386-433
- Oxycodone Hydrochloride10 mg/164380-260
- Oxycodone Hydrochloride20 mg/164380-262
- Oxycodone Hydrochloride30 mg/164380-263
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)