Cetirizine Hydrochloride 16571-0402
Product NDC
16571-0402- Manufacturer
- Rising Pharma Holdings, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- October 1, 2009
- Listing Expires
- December 31, 2027
- 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(3)
100 TABLET in 1 BOTTLE (16571-402-10)
300 TABLET in 1 BOTTLE (16571-402-30)
500 TABLET in 1 BOTTLE (16571-402-50)