NDC 58602-844 – Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride

Fexofenadine Hydrochloride 180 mg/1; Pseudoephedrine Hydrochloride 240 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Otc Drug

Product NDC58602-844

Product details

Brand name
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Generic name
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Labeler
Aurohealth LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA215232
Marketed since
April 17, 2025
Listing expires
December 31, 2026
Pharmacologic class
Histamine-1 Receptor Antagonist; alpha-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
58602-844-601 BLISTER PACK in 1 CARTON (58602-844-60) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKApr 17, 2025
58602-844-662 BLISTER PACK in 1 CARTON (58602-844-66) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKApr 17, 2025
58602-844-853 BLISTER PACK in 1 CARTON (58602-844-85) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKApr 17, 2025

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