NDC 45802-847 – Fexofenadine Hydrochloride
Fexofenadine Hydrochloride 180 mg/1 · Tablet, Film Coated · Oral
Product NDC45802-847
Product details
- Brand name
- Fexofenadine Hydrochloride
- Generic name
- fexofenadine hydrochloride
- Labeler
- Padagis Israel Pharmaceuticals Ltd
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 45802-847-78 | 1 BOTTLE in 1 CARTON (45802-847-78) / 100 TABLET, FILM COATED in 1 BOTTLE | Jan 7, 2022 |
Recalls mentioning this NDC
- D-0907-2023 Jul 19, 2023 · Class II
Failed Impurities/Degradation Specifications
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