NDC 30142-878 – Fexofenadine hydrochloride
Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral
Product NDC30142-878
Product details
- Brand name
- Fexofenadine hydrochloride
- Generic name
- Fexofenadine hydrochloride
- Labeler
- KROGER COMPANY
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076502
- Marketed since
- September 30, 2018
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 30142-878-15 | 3 BLISTER PACK in 1 CARTON (30142-878-15) / 5 TABLET in 1 BLISTER PACK | Sep 30, 2018 |
| 30142-878-30 | 1 BOTTLE in 1 CARTON (30142-878-30) / 30 TABLET in 1 BOTTLE | Sep 30, 2018 |
| 30142-878-64 | 2 BOTTLE in 1 CARTON (30142-878-64) / 70 TABLET in 1 BOTTLE | Jan 10, 2019 |
| 30142-878-70 | 1 BOTTLE in 1 CARTON (30142-878-70) / 70 TABLET in 1 BOTTLE | Sep 30, 2018 |
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