Class III ยท Low risk
FUROSEMIDE Tablets USP
CGMP Deviations: The active pharmaceutical ingredient (API) intended for use in furosemide oral solution USP was inadvertently used to manufacture the recalled furosemide tablets USP.
National Drug Code
Is NDC 0054-4299-31 recalled?
Furosemide · 1000 TABLET in 1 BOTTLE (0054-4299-31)
Yes — this exact package was recalled
1 FDA recall names the code 0054-4299-31 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
- Furosemide
- Strength
- FUROSEMIDE 40 mg/1
- Form
- Tablet · Oral
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Type
- Human Prescription Drug
- Product code
- 0054-4299
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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