Class II · Moderate risk
Buprenorphine HCl Injection
Sub-potent Drug: Out-of-Specification assay results found at 3 month stability testing.
National Drug Code
Is NDC 0143-9246-01 recalled?
Buprenorphine Hydrochloride
Yes — this exact package was recalled
1 FDA recall names the code 0143-9246-01 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.
- Active ingredient
- Buprenorphine Hydrochloride
- Strength
- BUPRENORPHINE HYDROCHLORIDE .324 mg/mL
- Form
- Injection · Intramuscular, Intravenous
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Type
- Human Prescription Drug · DEA CIII
- Product code
- 0143-9246
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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