Fexofenadine Hcl 72789-0196
Product NDC
72789-0196- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- February 18, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA204097
Active Ingredients
| Ingredient | Strength |
|---|---|
| Fexofenadine Hydrochloride | 180 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(3)
10 TABLET in 1 BOTTLE, PLASTIC (72789-196-10)
30 TABLET in 1 BOTTLE, PLASTIC (72789-196-30)
90 TABLET in 1 BOTTLE, PLASTIC (72789-196-90)