Fexofenadine Hcl 16714-0899
Product NDC
16714-0899- Manufacturer
- Northstar Rxllc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- February 18, 2019
- 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(2)
1 BOTTLE in 1 CARTON (16714-899-01) / 30 TABLET in 1 BOTTLE
1 BOTTLE in 1 CARTON (16714-899-02) / 100 TABLET in 1 BOTTLE