NDC 68210-2210 – Fexofenadine Hydrochloride
Fexofenadine Hydrochloride 180 mg/1 · Tablet, Film Coated · Oral
Product NDC68210-2210
Product details
- Brand name
- Fexofenadine Hydrochloride
- Generic name
- Fexofenadine Hydrochloride
- Labeler
- SPIRIT PHARMACEUTICALS LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204507
- Marketed since
- March 17, 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 Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68210-2210-1 | 100 TABLET, FILM COATED in 1 PACKAGE (68210-2210-1) | Mar 17, 2020 |
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