Fexofenadine Hydrochloride 73629-0008
Product NDC
73629-0008- Manufacturer
- Amz789 Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- July 27, 2024
- Listing Expires
- December 31, 2027
- 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, FILM COATED in 1 BOTTLE, PLASTIC (73629-008-03)