NDCFind

Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride 51660-0037-31

Package NDC

51660-0037-31

Product NDC: 51660-0037

Manufacturer
Ohm Laboratories Inc.
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Product Type
Human Otc Drug
Marketing Start
March 1, 2018
Listing Expires
December 31, 2026
Application
ANDA090818

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

51660-0037-31Selected

1 BLISTER PACK in 1 CARTON (51660-037-31) / 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Other packages for this product(1)

1 BLISTER PACK in 1 CARTON (51660-037-21) / 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK