NDC 51316-015 – Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride

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

Human Otc Drug

Product NDC51316-015

Product details

Brand name
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Generic name
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Labeler
CVS Health Corp
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA215434
Marketed since
June 3, 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
51316-015-204 BLISTER PACK in 1 CARTON (51316-015-20) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMar 17, 2023
51316-015-306 BLISTER PACK in 1 CARTON (51316-015-30) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMar 17, 2023

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