NDC 81469-353 – Cetirizine Hydrochloride
Cetirizine Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC81469-353
Product details
- Brand name
- Cetirizine Hydrochloride
- Generic name
- Cetirizine Hydrochloride
- Labeler
- First Nation Group, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076047
- Marketed since
- May 29, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Cetirizine Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Cetirizine hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 81469-353-01 | 100 TABLET in 1 BOTTLE (81469-353-01) | Jun 1, 2026 |
| 81469-353-03 | 300 TABLET in 1 BOTTLE (81469-353-03) | Jun 1, 2026 |
| 81469-353-05 | 500 TABLET in 1 BOTTLE (81469-353-05) | Jun 1, 2026 |
| 81469-353-90 | 90 TABLET in 1 BOTTLE (81469-353-90) | Jun 1, 2026 |
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