Class II ยท 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 10702-0018 recalled?
Oxycodone Hydrochloride
This product was recalled — in other package sizes
No FDA recall names your exact package code, but 1 recall cover the same product (10702-0018) in a different bottle or carton size. Worth checking with your pharmacist.
1 of these recalls is still ongoing.
- Active ingredient
- Oxycodone Hydrochloride
- Strength
- OXYCODONE HYDROCHLORIDE 5 mg/1
- Form
- Tablet · Oral
- Labeler
- Kvk-Tech,inc
- Type
- Human Prescription Drug · DEA CII
- Product code
- 10702-0018
Recalls of this product
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
- 10702-0026 Phentermine Hydrochloride 3
- 10702-0028 Phentermine Hydrochloride 2
- 10702-0040 Benzphetamine Hydrochloride 2
- 10702-0052 See recall 2
- 10702-0010 Hydroxyzine Hydrochloride 1
- 10702-0011 Hydroxyzine Hydrochloride 1
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