Fexofenadine Hcl 00904-7192
Product NDC
00904-7192- Manufacturer
- Major Pharmaceuticals
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- August 26, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA204507
Active Ingredients
| Ingredient | Strength |
|---|---|
| Fexofenadine Hydrochloride | 60 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(3)
100 TABLET, FILM COATED in 1 BOTTLE (0904-7192-04)
500 TABLET, FILM COATED in 1 BOTTLE (0904-7192-40)
100 TABLET, FILM COATED in 1 BOTTLE (0904-7192-60)