Fexofenadine Hcl 68788-7449
Product NDC
68788-7449- Manufacturer
- Preferred Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- August 19, 2016
- Listing Expires
- December 31, 2027
- Application
- ANDA204097
Active Ingredients
| Ingredient | Strength |
|---|---|
| Fexofenadine Hydrochloride | 180 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(4)
100 TABLET in 1 BOTTLE (68788-7449-1)
30 TABLET in 1 BOTTLE (68788-7449-3)
60 TABLET in 1 BOTTLE (68788-7449-6)
90 TABLET in 1 BOTTLE (68788-7449-9)