Fexofenadine Hydrochloride 69842-0052
Product NDC
69842-0052- Manufacturer
- Cvs Health Corp.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- April 1, 2011
- Listing Expires
- December 31, 2026
- Application
- ANDA076502
Active Ingredients
| Ingredient | Strength |
|---|---|
| Fexofenadine Hydrochloride | 180 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(7)
3 BLISTER PACK in 1 CARTON (69842-052-15) / 5 TABLET in 1 BLISTER PACK
1 CARTON in 1 CARTON (69842-052-18) / 180 TABLET in 1 CARTON
3 BLISTER PACK in 1 CARTON (69842-052-29) / 15 TABLET in 1 BLISTER PACK
1 BOTTLE in 1 CARTON (69842-052-30) / 30 TABLET in 1 BOTTLE
1 BOTTLE in 1 CARTON (69842-052-45) / 45 TABLET in 1 BOTTLE
1 BOTTLE in 1 CARTON (69842-052-70) / 70 TABLET in 1 BOTTLE
1 BOTTLE in 1 CARTON (69842-052-90) / 90 TABLET in 1 BOTTLE