Fexofenadine Hcl 71335-2165
Product NDC
71335-2165- Manufacturer
- Bryant Ranch Prepack
- 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(7)
30 TABLET, FILM COATED in 1 BOTTLE (71335-2165-1)
10 TABLET, FILM COATED in 1 BOTTLE (71335-2165-2)
60 TABLET, FILM COATED in 1 BOTTLE (71335-2165-3)
90 TABLET, FILM COATED in 1 BOTTLE (71335-2165-4)
14 TABLET, FILM COATED in 1 BOTTLE (71335-2165-5)
20 TABLET, FILM COATED in 1 BOTTLE (71335-2165-6)
12 TABLET, FILM COATED in 1 BOTTLE (71335-2165-7)