Fexofenadine Hydrochloride 68210-2210
Product NDC
68210-2210- Manufacturer
- Spirit Pharmaceuticals Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- March 17, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA204507
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, FILM COATED in 1 PACKAGE (68210-2210-1)