NDC 37808-022 – Fexofenadine HCl and Pseudoephedrine HCI
Fexofenadine Hydrochloride 60 mg/1; Pseudoephedrine Hydrochloride 120 mg/1 · Tablet, Extended Release · Oral
Product NDC37808-022
Product details
- Brand name
- Fexofenadine HCl and Pseudoephedrine HCI
- Generic name
- Fexofenadine HCl and Pseudoephedrine HCI
- Labeler
- HEB
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA076667
- Marketed since
- December 21, 2015
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 37808-022-31 | 6 BLISTER PACK in 1 CARTON (37808-022-31) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Dec 21, 2015 |
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