Class III · Low risk
Oxycodone Hydrochloride Tablets
Labeling; Label Error Not Elsewhere Classified; label missing controlled substance CII symbol
National Drug Code
Is NDC 31722-0917-01 recalled?
Oxycodone Hydrochloride · 100 TABLET in 1 BOTTLE (31722-917-01)
Yes — this exact package was recalled
1 FDA recall names the code 31722-0917-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Oxycodone Hydrochloride
- Strength
- OXYCODONE HYDROCHLORIDE 15 mg/1
- Form
- Tablet · Oral
- Labeler
- Camber Pharmaceuticals Inc
- Type
- Human Prescription Drug · DEA CII
- Product code
- 31722-0917
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 31722-0726 Montelukast Sodium 3
- 31722-0713 Pantoprazole Sodium 2
- 31722-0270 See recall 1
- 31722-0307 Ketorolac Tromethamine 1
- 31722-0513 Simvastatin 1
- 31722-0525 Finasteride 1
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