Fexofenadine Hcl 50228-0202
Product NDC
50228-0202- Manufacturer
- Sciegen Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- December 26, 2014
- 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(4)
30 TABLET, FILM COATED in 1 BOTTLE (50228-202-01)
1000 TABLET, FILM COATED in 1 BOTTLE (50228-202-02)
30 TABLET, FILM COATED in 1 BOTTLE (50228-202-03)
1000 TABLET, FILM COATED in 1 BOTTLE (50228-202-04)