NDC 71399-8042 – Fexofenadine HCL
Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral
Product NDC71399-8042
Product details
- Brand name
- Fexofenadine HCL
- Generic name
- Fexofenadine HCL
- Labeler
- Akron Pharma Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA204507
- Marketed since
- September 9, 2020
- 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 HCL →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 71399-8042-1 | 100 TABLET in 1 BOTTLE (71399-8042-1) | Sep 9, 2020 |
| 71399-8042-3 | 30 TABLET in 1 BOTTLE (71399-8042-3) | Aug 9, 2024 |
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