Class III · Low risk
Loperamide HCL Tablets USP
Labeling Not Elsewhere Classified: The front panel indicates 24 caplets whereas the side panel indicates 12 caplets. The drug product carton contains 24 caplets.
National Drug Code
Is NDC 53943-0123-24 recalled?
Loperamide Hydrochloride · 24 TABLET in 1 BLISTER PACK (53943-123-24)
Yes — this exact package was recalled
1 FDA recall names the code 53943-0123-24 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
- Loperamide Hydrochloride
- Strength
- LOPERAMIDE HYDROCHLORIDE 2 mg/1
- Form
- Tablet · Oral
- Labeler
- Discount Drug Mart
- Type
- Human OTC Drug
- Product code
- 53943-0123
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
- 53943-0021 See recall 1
- 53943-0107 Multi Symptom Antacid 1
- 53943-0192 See recall 1
- 53943-0291 Ibuprofen 1
- 53943-0292 Ibuprofen 1
- 53943-0871 See recall 1
Free recall alerts
Know the day your medication is recalled
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