NDC 58602-426 – Fexofenadine Hydrochloride

Fexofenadine Hydrochloride 30 mg/5mL · Suspension · Oral

Human Otc Drug

Product NDC58602-426

Product details

Brand name
Fexofenadine Hydrochloride
Generic name
Fexofenadine Hydrochloride Oral
Labeler
Aurohealth LLC
Dosage form
Suspension
Route
Oral
Marketing category
ANDA · ANDA213466
Marketed since
May 23, 2023
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
58602-426-201 BOTTLE in 1 CARTON (58602-426-20) / 240 mL in 1 BOTTLEMay 23, 2023
58602-426-241 BOTTLE in 1 CARTON (58602-426-24) / 120 mL in 1 BOTTLEMay 23, 2023

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