NDC 71335-2165 – Fexofenadine hcl
Fexofenadine Hydrochloride 60 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-2165
Product details
- Brand name
- Fexofenadine hcl
- Generic name
- Fexofenadine hcl
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204507
- Marketed since
- August 26, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Fexofenadine Hydrochloride 60 mg/1
Uses, dosage, side effects and warnings for Fexofenadine HCL →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2165-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2165-1) | Sep 6, 2024 |
| 71335-2165-2 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-2165-2) | Aug 25, 2022 |
| 71335-2165-3 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2165-3) | Sep 6, 2024 |
| 71335-2165-4 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2165-4) | Sep 6, 2024 |
| 71335-2165-5 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-2165-5) | Sep 6, 2024 |
| 71335-2165-6 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-2165-6) | Sep 6, 2024 |
| 71335-2165-7 | 12 TABLET, FILM COATED in 1 BOTTLE (71335-2165-7) | Nov 8, 2022 |
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