NDC 73581-026 – Fexofenadine Hydrochloride
Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral
Product NDC73581-026
Product details
- Brand name
- Fexofenadine Hydrochloride
- Generic name
- Fexofenadine Hydrochloride
- Labeler
- YYBA Corp
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA211075
- Marketed since
- December 18, 2025
- Listing expires
- December 31, 2027
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 73581-026-01 | 10 TABLET in 1 BOTTLE (73581-026-01) | Dec 18, 2025 |
| 73581-026-10 | 100 TABLET in 1 BOTTLE (73581-026-10) | Dec 18, 2025 |
| 73581-026-20 | 200 TABLET in 1 BOTTLE (73581-026-20) | Dec 18, 2025 |
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