Class III · Low risk
Methadone Hydrochloride Tablets
Failed Tablet/Capsule Specifications: Illegible product identification for the unit dose configuration only.
National Drug Code
Is NDC 0054-0709-20 recalled?
Methadone Hydrochloride · 1 BLISTER PACK in 1 CARTON (0054-0709-20) / 100 TABLET in 1 BLISTER PACK
Yes — this exact package was recalled
1 FDA recall names the code 0054-0709-20 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
- Methadone Hydrochloride
- Strength
- METHADONE HYDROCHLORIDE 5 mg/1
- Form
- Tablet · Oral
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Type
- Human Prescription Drug · DEA CII
- Product code
- 0054-0709
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
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