Cetirizine Hydrochloride 81469-0353
Product NDC
81469-0353- Manufacturer
- First Nation Group, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- May 29, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA076047
Active Ingredients
| Ingredient | Strength |
|---|---|
| Cetirizine Hydrochloride | 10 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(4)
100 TABLET in 1 BOTTLE (81469-353-01)
300 TABLET in 1 BOTTLE (81469-353-03)
500 TABLET in 1 BOTTLE (81469-353-05)
90 TABLET in 1 BOTTLE (81469-353-90)