NDC 73581-012 – Fexofenadine
Fexofenadine Hydrochloride 60 mg/1 · Tablet · Oral
Product NDC73581-012
Product details
- Brand name
- Fexofenadine
- Generic name
- Fexofenadine
- Labeler
- YYBA Corp
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA219032
- Marketed since
- July 27, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Fexofenadine Hydrochloride 60 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 73581-012-01 | 100 TABLET in 1 BOTTLE (73581-012-01) | Sep 1, 2026 |
| 73581-012-02 | 200 TABLET in 1 BOTTLE (73581-012-02) | Sep 1, 2026 |
| 73581-012-06 | 60 TABLET in 1 BOTTLE (73581-012-06) | Sep 1, 2026 |