NDC 58602-877 – Fexofenadine Hydrochloride
Fexofenadine Hydrochloride 60 mg/1 · Tablet, Film Coated · Oral
Product NDC58602-877
Product details
- Brand name
- Fexofenadine Hydrochloride
- Generic name
- Fexofenadine Hydrochloride
- Labeler
- Aurohealth LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202039
- Marketed since
- October 13, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Fexofenadine Hydrochloride 60 mg/1
Uses, dosage, side effects and warnings for Fexofenadine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 58602-877-09 | 1 BOTTLE in 1 CARTON (58602-877-09) / 30 TABLET, FILM COATED in 1 BOTTLE | Oct 13, 2023 |
| 58602-877-40 | 500 TABLET, FILM COATED in 1 BOTTLE (58602-877-40) | Oct 13, 2023 |
| 58602-877-74 | 1 BLISTER PACK in 1 CARTON (58602-877-74) / 6 TABLET, FILM COATED in 1 BLISTER PACK | Oct 13, 2023 |
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