Class II · Moderate risk
Oxycodone Hydrochloride Oral Solution
Impurity failure at 0-time of the repackaged lot.
National Drug Code
Is NDC 60687-0406-77 recalled?
Oxycodone Hydrochloride · 4 TRAY in 1 CASE (60687-406-77) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-406-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-406-40)
Yes — this exact package was recalled
1 FDA recall names the code 60687-0406-77 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 5 mg/5mL
- Form
- Solution · Oral
- Labeler
- American Health Packaging
- Type
- Human Prescription Drug · DEA CII
- Product code
- 60687-0406
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
- 60687-0423 Clobazam 2
- 60687-0695 See recall 2
- 60687-0106 See recall 1
- 60687-0112 Anastrozole 1
- 60687-0133 See recall 1
- 60687-0139 See recall 1
Free recall alerts
Know the day your medication is recalled
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