NDC 0615-8648 – Fexofenadine Hydrochloride
Fexofenadine Hydrochloride 180 mg/1 · Tablet, Film Coated · Oral
Product NDC0615-8648
Product details
- Brand name
- Fexofenadine Hydrochloride
- Generic name
- Fexofenadine Hydrochloride
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA091567
- Marketed since
- April 29, 2022
- Listing expires
- December 31, 2027
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 0615-8648-39 | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8648-39) | Jun 23, 2026 |
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