Cetirizine Hydrochloride 00781-1684
Product NDC
00781-1684- Manufacturer
- Sandoz Inc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- December 27, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA077946
Active Ingredients
| Ingredient | Strength |
|---|---|
| Cetirizine Hydrochloride | 10 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(2)
100 TABLET in 1 BOTTLE (0781-1684-01)
30 TABLET in 1 BOX, UNIT-DOSE (0781-1684-64)