NDC 70677-1009 – Fexofenadine Hydrochloride
Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral
Product NDC70677-1009
Product details
- Brand name
- Fexofenadine Hydrochloride
- Generic name
- Fexofenadine hydrochloride
- Labeler
- Strategic Sourcing Services, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076502
- Marketed since
- September 9, 2019
- 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 |
|---|---|---|
| 70677-1009-1 | 3 BLISTER PACK in 1 CARTON (70677-1009-1) / 5 TABLET in 1 BLISTER PACK | May 5, 2023 |
| 70677-1009-2 | 1 BOTTLE in 1 CARTON (70677-1009-2) / 30 TABLET in 1 BOTTLE | May 5, 2023 |
| 70677-1009-3 | 1 BOTTLE in 1 CARTON (70677-1009-3) / 70 TABLET in 1 BOTTLE | May 5, 2023 |
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