NDC 71335-2126
Oxycodone Hydrochloride 30 mg tablet
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-918.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ascent Pharmaceuticals Inc | Central Islip, NY, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyAug 9, 2024 · 9 inspections |
Repackaging site
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
Recalls
- Jan 22, 2018 · Class III · Ascent Pharmaceuticals, Inc.
Labeling; Label Error Not Elsewhere Classified; label missing controlled substance CII symbol
Lots: Lot Numbers: 17080591 and 17080619, exp 07/19; 17110907 and 17110908, exp 10/19; and 17120986, exp 11/19
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Oxycodone: every company that makes it
- Form
- tablet, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA207418
- On the market since
- Aug 8, 2017
- Package NDCs
71335-2126-171335-2126-271335-2126-371335-2126-471335-2126-571335-2126-671335-2126-771335-2126-8- Official label
- DailyMed (National Library of Medicine), updated May 29, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?