NDC 46122-779 – Fexofenadine Hydrochloride

Fexofenadine Hydrochloride 180 mg/1 · Tablet, Film Coated · Oral

Human Otc Drug

Product NDC46122-779

Product details

Brand name
Fexofenadine Hydrochloride
Generic name
Fexofenadine Hydrochloride
Labeler
AMERISOURCE BERGEN
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091567
Marketed since
May 14, 2024
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 (3)

Package NDCDescriptionSince
46122-779-583 BLISTER PACK in 1 CARTON (46122-779-58) / 5 TABLET, FILM COATED in 1 BLISTER PACKMay 14, 2024
46122-779-611 BOTTLE in 1 CARTON (46122-779-61) / 30 TABLET, FILM COATED in 1 BOTTLEMay 14, 2024
46122-779-661 BOTTLE in 1 CARTON (46122-779-66) / 90 TABLET, FILM COATED in 1 BOTTLEMay 14, 2024

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