Cetirizine Hydrochloride 71205-0164
Product NDC
71205-0164- Manufacturer
- Proficient Rx Lp
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- October 1, 2009
- 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(4)
15 TABLET in 1 BOTTLE (71205-164-15)
30 TABLET in 1 BOTTLE (71205-164-30)
60 TABLET in 1 BOTTLE (71205-164-60)
90 TABLET in 1 BOTTLE (71205-164-90)