Fexofenadine Hydrochloride 55111-0782
Product NDC
55111-0782- Manufacturer
- Dr. Reddy's Laboratories Limited
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- January 3, 2011
- Listing Expires
- December 31, 2026
- Application
- ANDA076502
Active Ingredients
| Ingredient | Strength |
|---|---|
| Fexofenadine Hydrochloride | 30 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(4)
100 TABLET in 1 BOTTLE (55111-782-01)
30 TABLET in 1 BOTTLE (55111-782-30)
10 BLISTER PACK in 1 CARTON (55111-782-78) / 10 TABLET in 1 BLISTER PACK (55111-782-79)
90 TABLET in 1 BOTTLE (55111-782-90)