NDC 11822-0021 – Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Fexofenadine Hydrochloride 60 mg/1; Pseudoephedrine Hydrochloride 120 mg/1 · Tablet, Extended Release · Oral
Product NDC11822-0021
Product details
- Brand name
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
- Generic name
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
- Labeler
- Rite Aid Corporation
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA215434
- Marketed since
- March 31, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-1 Receptor Antagonist; alpha-Adrenergic Agonist
Active ingredients
- Fexofenadine Hydrochloride 60 mg/1
- Pseudoephedrine Hydrochloride 120 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 11822-0021-4 | 4 BLISTER PACK in 1 CARTON (11822-0021-4) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Mar 31, 2023 |
| 11822-0021-6 | 6 BLISTER PACK in 1 CARTON (11822-0021-6) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Jul 23, 2023 |
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