Class II ยท Moderate risk
Furosemide Tablets
CGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit.
National Drug Code
Is NDC 69315-0118-01 recalled?
Furosemide · 100 TABLET in 1 BOTTLE (69315-118-01)
Yes — this exact package was recalled
1 FDA recall names the code 69315-0118-01 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.
1 of these recalls is still ongoing.
- Active ingredient
- Furosemide
- Strength
- FUROSEMIDE 80 mg/1
- Form
- Tablet · Oral
- Labeler
- Leading Pharma, LLC
- Type
- Human Prescription Drug
- Product code
- 69315-0118
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
- 69315-0308 ciprofloxacin 3
- 69315-0904 Lorazepam 2
- 69315-0127 Folic Acid 1
- 69315-0167 Clomipramine Hydrochloride 1
- 69315-0905 Lorazepam 1
- 69315-0906 Lorazepam 1
Free recall alerts
Know the day your medication is recalled
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