NDC 73581-025 – Fexofenadine Hydrochloride

Fexofenadine Hydrochloride 60 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC73581-025

Product details

Brand name
Fexofenadine Hydrochloride
Generic name
Fexofenadine Hydrochloride
Labeler
YYBA Corp
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211075
Marketed since
December 18, 2025
Listing expires
December 31, 2027
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
73581-025-0110 TABLET in 1 BOTTLE (73581-025-01)Dec 18, 2025
73581-025-0660 TABLET in 1 BOTTLE (73581-025-06)Dec 18, 2025
73581-025-20200 TABLET in 1 BOTTLE (73581-025-20)Dec 18, 2025

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