NDC 0363-2110 – Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride

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

Human Otc Drug

Product NDC0363-2110

Product details

Brand name
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Generic name
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Labeler
walgreens
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090818
Marketed since
April 17, 2018
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
0363-2110-2020 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0363-2110-20)Apr 17, 2018
0363-2110-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0363-2110-30)Apr 17, 2018

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