NDC 51655-231 – Fexofenadine Hydrochloride
Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral
Product NDC51655-231
Product details
- Brand name
- Fexofenadine Hydrochloride
- Generic name
- Fexofenadine HCl
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA204507
- Marketed since
- November 16, 2022
- Marketing end
- October 28, 2026
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Fexofenadine Hydrochloride 180 mg/1
Uses, dosage, side effects and warnings for Fexofenadine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51655-231-26 | 90 TABLET in 1 BOTTLE, PLASTIC (51655-231-26) | Dec 8, 2022 |
| 51655-231-52 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-231-52) | Nov 16, 2022 |
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