NDC 51655-231 – Fexofenadine Hydrochloride

Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC51655-231

Product details

Brand name
Fexofenadine Hydrochloride
Generic name
Fexofenadine HCl
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204507
Marketed since
November 16, 2022
Marketing end
October 28, 2026
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
51655-231-2690 TABLET in 1 BOTTLE, PLASTIC (51655-231-26)Dec 8, 2022
51655-231-5230 TABLET in 1 BOTTLE, PLASTIC (51655-231-52)Nov 16, 2022

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