NDCFind

Fexofenadine Hcl And Pseudoephedrine Hci 37808-0022-31

Package NDC

37808-0022-31

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

IngredientStrength
Fexofenadine Hydrochloride60 mg/1
Pseudoephedrine Hydrochloride120 mg/1

Drug Class

Adrenergic alpha-Agonists [MoA]Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]

Selected Package

37808-0022-31Selected

6 BLISTER PACK in 1 CARTON (37808-022-31) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK