NDC 79481-0847 – Allergy relief
Fexofenadine Hydrochloride 180 mg/1 · Tablet, Film Coated · Oral
Product NDC79481-0847
Product details
- Brand name
- Allergy relief
- Generic name
- Fexofenadine hydrochloride
- Labeler
- Meijer, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA212971
- Marketed since
- October 6, 2021
- 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 Allergy Relief →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 79481-0847-0 | 15 BLISTER PACK in 1 CARTON (79481-0847-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK | Oct 18, 2021 |
| 79481-0847-1 | 1 BOTTLE in 1 CARTON (79481-0847-1) / 30 TABLET, FILM COATED in 1 BOTTLE | Oct 6, 2021 |
| 79481-0847-2 | 1 BOTTLE in 1 CARTON (79481-0847-2) / 45 TABLET, FILM COATED in 1 BOTTLE | Oct 18, 2021 |
| 79481-0847-3 | 1 BOTTLE in 1 CARTON (79481-0847-3) / 40 TABLET, FILM COATED in 1 BOTTLE | Jul 25, 2024 |
| 79481-0847-4 | 1 BOTTLE in 1 CARTON (79481-0847-4) / 90 TABLET, FILM COATED in 1 BOTTLE | Jun 14, 2024 |
Recalls mentioning this NDC
- D-0906-2023 Jul 19, 2023 · Class II
Failed Impurities/Degradation Specifications
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