NDC 72090-010 – Fexofenadine Hydrochloride
Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral
Product NDC72090-010
Product details
- Brand name
- Fexofenadine Hydrochloride
- Generic name
- Fexofenadine Hydrochloride
- Labeler
- Pioneer Life Sciences, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA210137
- Marketed since
- October 3, 2024
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 72090-010-01 | 90 TABLET in 1 BOTTLE (72090-010-01) | Dec 7, 2023 |
| 72090-010-02 | 100 TABLET in 1 BOTTLE (72090-010-02) | Oct 29, 2024 |
| 72090-010-03 | 50 TABLET in 1 BOTTLE (72090-010-03) | Oct 3, 2024 |
| 72090-010-04 | 150 TABLET in 1 BOTTLE (72090-010-04) | Oct 3, 2024 |
| 72090-010-99 | 1000 TABLET in 1 BOTTLE (72090-010-99) | Aug 11, 2023 |
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