Fexofenadine Hydrochloride 00904-6711
Product NDC
00904-6711- Manufacturer
- Major Pharmaceuticals
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- April 27, 2018
- Application
- ANDA076502
Active Ingredients
| Ingredient | Strength |
|---|---|
| Fexofenadine Hydrochloride | 180 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(1)
1 BOTTLE in 1 CARTON (0904-6711-46) / 30 TABLET in 1 BOTTLE