NDC 51672-2141 – Childrens Fexofenadine Hydrochloride Allergy
Fexofenadine Hydrochloride 30 mg/5mL · Suspension · Oral
Product NDC51672-2141
Product details
- Brand name
- Childrens Fexofenadine Hydrochloride Allergy
- Generic name
- Fexofenadine Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Suspension
- Route
- Oral
- Marketing category
- ANDA · ANDA208123
- Marketed since
- January 24, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Fexofenadine Hydrochloride 30 mg/5mL
Uses, dosage, side effects and warnings for Childrens Fexofenadine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51672-2141-1 | 1 BOTTLE in 1 CARTON (51672-2141-1) / 240 mL in 1 BOTTLE | Jan 24, 2024 |
| 51672-2141-8 | 1 BOTTLE in 1 CARTON (51672-2141-8) / 120 mL in 1 BOTTLE | Jan 24, 2024 |