NDC 0904-7050 – Fexofenadine Hydrochloride

Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC0904-7050

Product details

Brand name
Fexofenadine Hydrochloride
Generic name
Fexofenadine HCl
Labeler
Major Pharmaceuticals
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204507
Marketed since
November 29, 2019
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
0904-7050-40500 TABLET in 1 BOTTLE, PLASTIC (0904-7050-40)Nov 29, 2019
0904-7050-60100 TABLET in 1 BOTTLE, PLASTIC (0904-7050-60)Nov 29, 2019

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