NDC 0363-1606 – Fexofenadine HCl and Pseudoephedrine HCI
Fexofenadine Hydrochloride 60 mg/1; Pseudoephedrine Hydrochloride 120 mg/1 · Tablet, Extended Release · Oral
Product NDC0363-1606
Product details
- Brand name
- Fexofenadine HCl and Pseudoephedrine HCI
- Generic name
- Fexofenadine HCl and Pseudoephedrine HCI
- Labeler
- Walgreens Company
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA076667
- Marketed since
- September 16, 2019
- 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
Uses, dosage, side effects and warnings for Fexofenadine HCl and Pseudoephedrine HCI →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0363-1606-20 | 4 BLISTER PACK in 1 CARTON (0363-1606-20) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Sep 16, 2019 |
| 0363-1606-30 | 6 BLISTER PACK in 1 CARTON (0363-1606-30) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Sep 16, 2019 |
Recalls mentioning this NDC
- D-0378-2022 Jan 26, 2022 · Class III
Failed Dissolution Specifications
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