NDC 73581-010 – Fexofenadine HCL

Fexofenadine Hydrochloride 60 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC73581-010

Product details

Brand name
Fexofenadine HCL
Generic name
Fexofenadine HCL
Labeler
YYBA Corp
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204097
Marketed since
January 1, 2026
Listing expires
December 31, 2027
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
73581-010-0110 TABLET in 1 BOTTLE (73581-010-01)Jan 1, 2026
73581-010-0660 TABLET in 1 BOTTLE (73581-010-06)Jan 1, 2026
73581-010-10100 TABLET in 1 BOTTLE (73581-010-10)Jan 1, 2026
73581-010-20200 TABLET in 1 BOTTLE (73581-010-20)Jan 1, 2026

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