Childrens Fexofenadine Hydrochloride Allergy 51672-2141
Generic: Fexofenadine Hydrochloride
Product NDC
51672-2141- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Suspension
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- January 24, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA208123
Active Ingredients
| Ingredient | Strength |
|---|---|
| Fexofenadine Hydrochloride | 30 mg/5mL |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(2)
1 BOTTLE in 1 CARTON (51672-2141-1) / 240 mL in 1 BOTTLE
1 BOTTLE in 1 CARTON (51672-2141-8) / 120 mL in 1 BOTTLE