Fexofenadine Hydrochloride 71205-0739
Product NDC
71205-0739- Manufacturer
- Proficient Rx Lp
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- January 7, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA212971
Active Ingredients
| Ingredient | Strength |
|---|---|
| Fexofenadine Hydrochloride | 180 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(3)
30 TABLET, FILM COATED in 1 BOTTLE (71205-739-30)
60 TABLET, FILM COATED in 1 BOTTLE (71205-739-60)
90 TABLET, FILM COATED in 1 BOTTLE (71205-739-90)