Cetirizine Hydrochloride 85293-0001
Product NDC
85293-0001- Manufacturer
- Umasuto, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- March 4, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA077829
Active Ingredients
| Ingredient | Strength |
|---|---|
| Cetirizine Hydrochloride | 10 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(1)
100 TABLET in 1 BOTTLE (85293-001-01)