NDC 71335-1217 – Fexofenadine HCL
Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral
Product NDC71335-1217
Product details
- Brand name
- Fexofenadine HCL
- Generic name
- Fexofenadine HCL
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA204097
- Marketed since
- August 19, 2016
- 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 (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1217-1 | 30 TABLET in 1 BOTTLE (71335-1217-1) | May 14, 2019 |
| 71335-1217-2 | 15 TABLET in 1 BOTTLE (71335-1217-2) | May 14, 2019 |
| 71335-1217-3 | 60 TABLET in 1 BOTTLE (71335-1217-3) | May 14, 2019 |
| 71335-1217-4 | 90 TABLET in 1 BOTTLE (71335-1217-4) | May 14, 2019 |
| 71335-1217-5 | 5 TABLET in 1 BOTTLE (71335-1217-5) | May 14, 2019 |
| 71335-1217-6 | 180 TABLET in 1 BOTTLE (71335-1217-6) | May 14, 2019 |
| 71335-1217-7 | 100 TABLET in 1 BOTTLE (71335-1217-7) | May 14, 2019 |
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