Class II · Moderate risk
Methadone Hydrochloride Oral Concentrate
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
National Drug Code
Is NDC 66689-0711-16 recalled?
Methadone Hydrochloride
Yes — this exact package was recalled
1 FDA recall names the code 66689-0711-16 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
- Methadone Hydrochloride
- Strength
- METHADONE HYDROCHLORIDE 5 mg/5mL
- Form
- Solution · Oral
- Labeler
- VistaPharm, LLC
- Type
- Human Prescription Drug · DEA CII
- Product code
- 66689-0711
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
- 66689-0037 See recall 5
- 66689-0008 See recall 4
- 66689-0023 See recall 3
- 66689-0031 See recall 3
- 66689-0036 See recall 3
- 66689-0038 See recall 3
Free recall alerts
Know the day your medication is recalled
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