NDC 84324-008 – Fexofenadine Hydrochloride

Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC84324-008

Product details

Brand name
Fexofenadine Hydrochloride
Generic name
Fexofenadine Hydrochloride
Labeler
NUVICARE LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210137
Marketed since
June 9, 2025
Listing expires
December 31, 2026
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
84324-008-0118 TABLET in 1 BOTTLE (84324-008-01)Jul 17, 2024
84324-008-024 TABLET in 1 BLISTER PACK (84324-008-02)Jun 9, 2025

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