NDC 16571-401 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 5 mg/1 · Tablet · Oral
Product NDC16571-401
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077829
- Marketed since
- October 1, 2009
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Cetirizine Hydrochloride 5 mg/1
Uses, dosage, side effects and warnings for Cetirizine hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 16571-401-10 | 100 TABLET in 1 BOTTLE (16571-401-10) | Oct 1, 2009 |
Recalls mentioning this NDC
- D-0732-2026 Jul 29, 2026 · Class I
Cross Contamination with Other Products: Customer complaints for appearance of discolored tablets and red dots observed on Cetirizine Hydrochloride Tablets USP 5 mg. Determined to be Ranitidine.
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