Cetirizine Hydrochloride 71335-0300
Product NDC
71335-0300- Manufacturer
- Bryant Ranch Prepack
- 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(9)
30 TABLET in 1 BOTTLE (71335-0300-1)
14 TABLET in 1 BOTTLE (71335-0300-2)
7 TABLET in 1 BOTTLE (71335-0300-3)
10 TABLET in 1 BOTTLE (71335-0300-4)
15 TABLET in 1 BOTTLE (71335-0300-5)
90 TABLET in 1 BOTTLE (71335-0300-6)
20 TABLET in 1 BOTTLE (71335-0300-7)
60 TABLET in 1 BOTTLE (71335-0300-8)
100 TABLET in 1 BOTTLE (71335-0300-9)