Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride 37808-0999
Product NDC
37808-0999- Manufacturer
- H E B
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- August 1, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA090818
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)
1 BLISTER PACK in 1 CARTON (37808-999-30) / 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
External Resources