Fexofenadine Hydrochloride 43598-0809
Product NDC
43598-0809- Manufacturer
- Dr. Reddy's Laboratories Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- December 26, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA076502
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 (43598-809-18) / 180 TABLET in 1 BOTTLE
1 BOTTLE in 1 CARTON (43598-809-90) / 90 TABLET in 1 BOTTLE