Class II · Moderate risk
Oxycodone Hydrochloride Tablets
Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.
National Drug Code
Is NDC 68084-0354-01 recalled?
Oxycodone Hydrochloride · 100 BLISTER PACK in 1 CARTON (68084-354-01) / 1 TABLET in 1 BLISTER PACK (68084-354-11)
Yes — this exact package was recalled
1 FDA recall names the code 68084-0354-01 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.
1 of these recalls is still ongoing.
- Active ingredient
- Oxycodone Hydrochloride
- Strength
- OXYCODONE HYDROCHLORIDE 5 mg/1
- Form
- Tablet · Oral
- Labeler
- American Health Packaging
- Type
- Human Prescription Drug · DEA CII
- Product code
- 68084-0354
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
- 68084-0295 See recall 3
- 68084-0446 See recall 3
- 68084-0214 Benzonatate 2
- 68084-0279 See recall 2
- 68084-0325 See recall 2
- 68084-0390 See recall 2
Free recall alerts
Know the day your medication is recalled
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