Fexofenadine Hcl 71399-8042
Product NDC
71399-8042- Manufacturer
- Akron Pharma Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- September 9, 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(2)
100 TABLET in 1 BOTTLE (71399-8042-1)
30 TABLET in 1 BOTTLE (71399-8042-3)