NDC 71205-739 – Fexofenadine Hydrochloride
Fexofenadine Hydrochloride 180 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-739
Product details
- Brand name
- Fexofenadine Hydrochloride
- Generic name
- Fexofenadine hydrochloride
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA212971
- Marketed since
- January 7, 2022
- 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 Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 71205-739-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-739-30) | Dec 28, 2022 |
| 71205-739-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-739-60) | Dec 28, 2022 |
| 71205-739-90 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-739-90) | Dec 28, 2022 |
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