Class II · Moderate risk
Amantadine Hydrochloride Tablets 100 mg 100-count bottle
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
National Drug Code
Is NDC 0832-0111-00 recalled?
Amantadine Hydrochloride · 100 TABLET in 1 BOTTLE (0832-0111-00)
Yes — this exact package was recalled
2 FDA recalls name the code 0832-0111-00 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
- amantadine hydrochloride
- Strength
- AMANTADINE HYDROCHLORIDE 100 mg/1
- Form
- Tablet · Oral
- Labeler
- Upsher-Smith Laboratories, LLC
- Type
- Human Prescription Drug
- Product code
- 0832-0111
Recalls naming this package
Class II · Moderate risk
Amantadine HCL
Labeling: Label Mixup: AMANTADINE HCL, Tablet, 100 mg may have potentially been mislabeled as one of the following drugs: MAGNESIUM CHLORIDE, Tablet, 64 mg, NDC 68585000575, Pedigree: AD52993_4, EXP: 5/17/2014; QUEtiapine FUMARATE, Tablet, 25 mg, NDC 65862048901, Pedigree: AD49582_22, EXP: 4/30/2014.
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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