Fexofenadine Hcl 71399-8659
Product NDC
71399-8659- Manufacturer
- Akron Pharma Inc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- December 26, 2014
- Listing Expires
- December 31, 2027
- 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(2)
100 TABLET, FILM COATED in 1 BOTTLE (71399-8659-1)
500 TABLET, FILM COATED in 1 BOTTLE (71399-8659-5)