Cetirizine Hydrochloride 71205-0207
Product NDC
71205-0207- Manufacturer
- Proficient Rx Lp
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- December 27, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA078336
Active Ingredients
| Ingredient | Strength |
|---|---|
| Cetirizine Hydrochloride | 10 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(6)
6 TABLET in 1 BOTTLE (71205-207-06)
10 TABLET in 1 BOTTLE (71205-207-10)
15 TABLET in 1 BOTTLE (71205-207-15)
30 TABLET in 1 BOTTLE (71205-207-30)
60 TABLET in 1 BOTTLE (71205-207-60)
90 TABLET in 1 BOTTLE (71205-207-90)