NDC 58602-427 – Fexofenadine Hydrochloride
Fexofenadine Hydrochloride 30 mg/5mL · Suspension · Oral
Product NDC58602-427
Product details
- Brand name
- Fexofenadine Hydrochloride
- Generic name
- Fexofenadine Hydrochloride Oral
- Labeler
- Aurohealth LLC
- Dosage form
- Suspension
- Route
- Oral
- Marketing category
- ANDA · ANDA213466
- Marketed since
- August 31, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Fexofenadine Hydrochloride 30 mg/5mL
Uses, dosage, side effects and warnings for Fexofenadine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 58602-427-20 | 1 BOTTLE in 1 CARTON (58602-427-20) / 240 mL in 1 BOTTLE | Aug 31, 2026 |
| 58602-427-24 | 1 BOTTLE in 1 CARTON (58602-427-24) / 120 mL in 1 BOTTLE | Aug 31, 2026 |
Other Fexofenadine Hydrochloride products
- 10202-229 Fexofenadine Hydrochloride 180 mg/1 · Tablet, Film Coated · 7-eleven
- 46122-779 Fexofenadine Hydrochloride 180 mg/1 · Tablet, Film Coated · AMERISOURCE BERGEN
- 73629-008 Fexofenadine Hydrochloride 180 mg/1 · Tablet, Film Coated · AMZ789 LLC
- 58602-876 Fexofenadine Hydrochloride 30 mg/1 · Tablet, Film Coated · Aurohealth LLC
- 58602-877 Fexofenadine Hydrochloride 60 mg/1 · Tablet, Film Coated · Aurohealth LLC
- 58602-878 Fexofenadine Hydrochloride 180 mg/1 · Tablet, Film Coated · Aurohealth LLC
- 58602-426 Fexofenadine Hydrochloride 30 mg/5mL · Suspension · Aurohealth LLC
- 68001-439 Fexofenadine Hydrochloride 60 mg/1 · Tablet · BluePoint Laboratories
- 68001-440 Fexofenadine Hydrochloride 180 mg/1 · Tablet · BluePoint Laboratories
- 82725-0102 Fexofenadine Hydrochloride 180 mg/1 · Tablet · Cabinet Health P.B.C.
- 68016-995 Fexofenadine Hydrochloride 180 mg/1 · Tablet · Chain Drug Consortium, LLC
- 63868-025 Fexofenadine Hydrochloride 180 mg/1 · Tablet · Chain Drug Marketing Associate