Fexofenadine Hcl 51316-0767
Product NDC
51316-0767- Manufacturer
- Cvs
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- March 27, 2024
- 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(1)
30 TABLET in 1 BOTTLE (51316-767-03)