Class II · Moderate risk
Lorazepam Tablets
Failed impurities/degradation specifications and Sub-potent Drug: Out-of-specification results were obtained during routine stability testing for Assay and Impurities.
National Drug Code
Is NDC 69315-0904-05 recalled?
Lorazepam · 500 TABLET in 1 BOTTLE (69315-904-05)
Yes — this exact package was recalled
1 FDA recall names the code 69315-0904-05 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
- Lorazepam
- Strength
- LORAZEPAM .5 mg/1
- Form
- Tablet · Oral
- Labeler
- Leading Pharma, LLC
- Type
- Human Prescription Drug · DEA CIV
- Product code
- 69315-0904
Recalls naming this package
Class II · Moderate risk
Lorazepam Tablets
Labeling: Label Error on Declared Strength. Bottle labeled as 0.5 mg tablets contained 1mg tablets of lorazepam
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
- 69315-0308 ciprofloxacin 3
- 69315-0118 Furosemide 1
- 69315-0127 Folic Acid 1
- 69315-0167 Clomipramine Hydrochloride 1
- 69315-0905 Lorazepam 1
- 69315-0906 Lorazepam 1
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