Fexofenadine Hcl 71335-1217
Product NDC
71335-1217- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- August 19, 2016
- Listing Expires
- December 31, 2026
- 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(7)
30 TABLET in 1 BOTTLE (71335-1217-1)
15 TABLET in 1 BOTTLE (71335-1217-2)
60 TABLET in 1 BOTTLE (71335-1217-3)
90 TABLET in 1 BOTTLE (71335-1217-4)
5 TABLET in 1 BOTTLE (71335-1217-5)
180 TABLET in 1 BOTTLE (71335-1217-6)
100 TABLET in 1 BOTTLE (71335-1217-7)