NDC 63304-222
Oxymorphone hydrochloride 20 mg tablet, film coated, extended release
On the label: Ranbaxy Laboratories Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ohm Laboratories Inc. | New Brunswick, NJ, United States | Makes it | No problems foundOct 31, 2024 · 22 inspections |
Product details
- Generic drug
- Oxymorphone: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 20 mg
- Approval
- ANDA ANDA203506
- On the market since
- Apr 13, 2015
- Package NDCs
63304-222-0563304-222-30- Official label
- DailyMed (National Library of Medicine), updated Sep 13, 2016
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?