Fexofenadine Hydrochloride 71309-0091
Product NDC
71309-0091- Manufacturer
- Safrel Pharmaceuticals, Llc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- January 3, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA211075
Active Ingredients
| Ingredient | Strength |
|---|---|
| Fexofenadine Hydrochloride | 180 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(1)
100 TABLET in 1 BOTTLE (71309-091-01)