Class III · Low risk
Levocetirizine Dihydrochloride Tablets
Failed Impurities/Degradation Specifications: One lot of Levocetirizine dihydrochloride tablets 5 mg 30 count failed stability testing.
National Drug Code
Is NDC 10135-0639-30 recalled?
Levocetirizine Dihydrochloride · 30 TABLET, FILM COATED in 1 BOTTLE (10135-639-30)
Yes — this exact package was recalled
1 FDA recall names the code 10135-0639-30 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
- levocetirizine Dihydrochloride
- Strength
- LEVOCETIRIZINE DIHYDROCHLORIDE 5 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Marlex Pharmaceuticals Inc
- Type
- Human Prescription Drug
- Product code
- 10135-0639
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
- 10135-0152 See recall 1
- 10135-0691 See recall 1
- 10135-0747 Digoxin 1
- 10135-0748 Digoxin 1
Free recall alerts
Know the day your medication is recalled
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