Fexofenadine Hydrochloride 62207-0891
Product NDC
62207-0891- Manufacturer
- Granules India Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- November 7, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA211075
Active Ingredients
| Ingredient | Strength |
|---|---|
| Fexofenadine Hydrochloride | 180 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(3)
1000 TABLET, FILM COATED in 1 BOTTLE (62207-891-49)
1 BOTTLE in 1 CARTON (62207-891-51) / 10 TABLET, FILM COATED in 1 BOTTLE
7 BLISTER PACK in 1 CARTON (62207-891-58) / 10 TABLET, FILM COATED in 1 BLISTER PACK