Fexofenadine Hydrochloride 12579-0181
Product NDC
12579-0181- Manufacturer
- Opella Healthcare International Sas
- Dosage Form
- Tablet, Film Coated, Extended Release
- Product Type
- Drug For Further Processing
- Marketing Start
- April 3, 2026
- Listing Expires
- December 31, 2027
Active Ingredients
| Ingredient | Strength |
|---|---|
| Fexofenadine Hydrochloride | 60 mg/1 |
Packaging Options(1)
560000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BAG (12579-181-01)