Class III · Low risk
Ohm Loratadine Orally Disintegrating Tablets
Superpotent Drug: Out Of Specification (OOS) result for Assay.
National Drug Code
Is NDC 51660-0527-31 recalled?
Allergy Relief · 30 BLISTER PACK in 1 CARTON (51660-527-31) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Yes — this exact package was recalled
1 FDA recall names the code 51660-0527-31 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
- Loratadine
- Strength
- LORATADINE 10 mg/1
- Form
- Tablet, Orally Disintegrating · Oral
- Labeler
- Ohm Laboratories Inc.
- Type
- Human OTC Drug
- Product code
- 51660-0527
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
- 51660-0998 Fexofenadine Hydrochloride 1
Free recall alerts
Know the day your medication is recalled
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