NDC 73581-009 – Fexofenadine HCL
Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral
Product NDC73581-009
Product details
- Brand name
- Fexofenadine HCL
- Generic name
- Fexofenadine HCL
- Labeler
- YYBA Corp
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA204097
- Marketed since
- August 19, 2016
- 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 HCL →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 73581-009-01 | 10 TABLET in 1 BOTTLE (73581-009-01) | Jan 1, 2026 |
| 73581-009-04 | 40 TABLET in 1 BOTTLE (73581-009-04) | Jan 1, 2026 |
| 73581-009-10 | 100 TABLET in 1 BOTTLE (73581-009-10) | Jan 1, 2026 |
| 73581-009-20 | 200 TABLET in 1 BOTTLE (73581-009-20) | Jan 1, 2026 |
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