NDC 79481-6230 – Fexofenadine HCL

Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC79481-6230

Product details

Brand name
Fexofenadine HCL
Generic name
Fexofenadine HCL
Labeler
Meijer, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211075
Marketed since
July 1, 2024
Listing expires
December 31, 2026
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Fexofenadine HCL →

Package NDC codes (2)

Package NDCDescriptionSince
79481-6230-224 TABLET in 1 BOTTLE (79481-6230-2)Aug 1, 2025
79481-6230-660 TABLET in 1 BOTTLE (79481-6230-6)Jul 1, 2024

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