Class III · Low risk
Cetirizine Hydrochloride Tablets USP 10 mg
Tablet/Capsules Imprinted with Wrong ID
National Drug Code
Is NDC 16571-0402-50 recalled?
Cetirizine Hydrochloride · 500 TABLET in 1 BOTTLE (16571-402-50)
Yes — this exact package was recalled
1 FDA recall names the code 16571-0402-50 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.
2 of these recalls are still ongoing.
- Active ingredient
- Cetirizine Hydrochloride
- Strength
- CETIRIZINE HYDROCHLORIDE 10 mg/1
- Form
- Tablet · Oral
- Labeler
- Rising Pharma Holdings, Inc.
- Type
- Human OTC Drug
- Product code
- 16571-0402
Recalls naming this package
Class III · Low risk
Cetirizine Hydrochloride Tablets USP 10 mg
Tablet/Capsules Imprinted with Wrong ID
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
- 16571-0130 See recall 2
- 16571-0140 See recall 2
- 16571-0141 See recall 2
- 16571-0742 See recall 2
- 16571-0301 See recall 1
- 16571-0302 See recall 1
Free recall alerts
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