NDC 51316-800 – Fexofenadine Hydrochloride
Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral
Product NDC51316-800
Product details
- Brand name
- Fexofenadine Hydrochloride
- Generic name
- Fexofenadine Hydrochloride
- Labeler
- CVS PHARMACY, INC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA091567
- Marketed since
- September 20, 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 (6)
| Package NDC | Description | Since |
|---|---|---|
| 51316-800-08 | 1 BOTTLE in 1 CARTON (51316-800-08) / 180 TABLET in 1 BOTTLE | Sep 20, 2022 |
| 51316-800-15 | 1 BLISTER PACK in 1 CARTON (51316-800-15) / 15 TABLET in 1 BLISTER PACK | Sep 20, 2022 |
| 51316-800-30 | 1 BOTTLE in 1 CARTON (51316-800-30) / 30 TABLET in 1 BOTTLE | Sep 20, 2022 |
| 51316-800-45 | 1 BOTTLE in 1 CARTON (51316-800-45) / 45 TABLET in 1 BOTTLE | Sep 20, 2022 |
| 51316-800-70 | 1 BOTTLE in 1 CARTON (51316-800-70) / 70 TABLET in 1 BOTTLE | Sep 20, 2022 |
| 51316-800-90 | 1 BOTTLE in 1 CARTON (51316-800-90) / 90 TABLET in 1 BOTTLE | Sep 20, 2022 |
Recalls mentioning this NDC
- D-0273-2024 Jan 31, 2024 · Class II
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
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