Fexofenadine Hcl And Pseudoephedrine Hci 37808-0022
Product NDC
37808-0022- Manufacturer
- Heb
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- December 21, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA076667
Active Ingredients
| Ingredient | Strength |
|---|---|
| Fexofenadine Hydrochloride | 60 mg/1 |
| Pseudoephedrine Hydrochloride | 120 mg/1 |
Drug Class
Adrenergic alpha-Agonists [MoA]Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(1)
6 BLISTER PACK in 1 CARTON (37808-022-31) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK