Cetirizine Hydrochloride 70692-0139
Product NDC
70692-0139- Manufacturer
- Strive Pharmaceuticals Inc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- July 1, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA209274
Active Ingredients
| Ingredient | Strength |
|---|---|
| Cetirizine Hydrochloride | 10 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(1)
14 TABLET in 1 BOTTLE (70692-139-14)