Class II · Moderate risk
Alendronate Sodium Oral Solution
This recall is being conducted due to out of specification assay results in a limited number of bottles that were stored on side.
National Drug Code
Is NDC 0054-0282-59 recalled?
Alendronate Sodium · 4 BOTTLE, UNIT-DOSE in 1 CARTON (0054-0282-59) / 75 mL in 1 BOTTLE, UNIT-DOSE
Yes — this exact package was recalled
1 FDA recall names the code 0054-0282-59 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
- Alendronate Sodium
- Strength
- ALENDRONATE SODIUM 70 mg/75mL
- Form
- Solution · Oral
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Type
- Human Prescription Drug
- Product code
- 0054-0282
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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