NDC 0363-0044 – Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride

Fexofenadine Hydrochloride 60 mg/1; Pseudoephedrine Hydrochloride 120 mg/1 · Tablet, Extended Release · Oral

Human Otc Drug

Product NDC0363-0044

Product details

Brand name
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Generic name
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Labeler
Walgreens Company
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA215434
Marketed since
March 31, 2022
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 (2)

Package NDCDescriptionSince
0363-0044-204 BLISTER PACK in 1 CARTON (0363-0044-20) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMar 31, 2023
0363-0044-306 BLISTER PACK in 1 CARTON (0363-0044-30) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMar 31, 2023

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