NDC 72090-010 – Fexofenadine Hydrochloride

Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC72090-010

Product details

Brand name
Fexofenadine Hydrochloride
Generic name
Fexofenadine Hydrochloride
Labeler
Pioneer Life Sciences, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210137
Marketed since
October 3, 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 (5)

Package NDCDescriptionSince
72090-010-0190 TABLET in 1 BOTTLE (72090-010-01)Dec 7, 2023
72090-010-02100 TABLET in 1 BOTTLE (72090-010-02)Oct 29, 2024
72090-010-0350 TABLET in 1 BOTTLE (72090-010-03)Oct 3, 2024
72090-010-04150 TABLET in 1 BOTTLE (72090-010-04)Oct 3, 2024
72090-010-991000 TABLET in 1 BOTTLE (72090-010-99)Aug 11, 2023

Other Fexofenadine Hydrochloride products