NDC 46122-779 – Fexofenadine Hydrochloride
Fexofenadine Hydrochloride 180 mg/1 · Tablet, Film Coated · Oral
Product NDC46122-779
Product details
- Brand name
- Fexofenadine Hydrochloride
- Generic name
- Fexofenadine Hydrochloride
- Labeler
- AMERISOURCE BERGEN
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA091567
- Marketed since
- May 14, 2024
- Listing expires
- December 31, 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 46122-779-58 | 3 BLISTER PACK in 1 CARTON (46122-779-58) / 5 TABLET, FILM COATED in 1 BLISTER PACK | May 14, 2024 |
| 46122-779-61 | 1 BOTTLE in 1 CARTON (46122-779-61) / 30 TABLET, FILM COATED in 1 BOTTLE | May 14, 2024 |
| 46122-779-66 | 1 BOTTLE in 1 CARTON (46122-779-66) / 90 TABLET, FILM COATED in 1 BOTTLE | May 14, 2024 |
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