NDC 71205-531 – Fexofenadine HCL

Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC71205-531

Product details

Brand name
Fexofenadine HCL
Generic name
Fexofenadine HCL
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204097
Marketed since
August 19, 2016
Listing expires
December 31, 2026
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
71205-531-1010 TABLET in 1 BOTTLE (71205-531-10)Mar 11, 2024
71205-531-1515 TABLET in 1 BOTTLE (71205-531-15)Mar 11, 2024
71205-531-2020 TABLET in 1 BOTTLE (71205-531-20)Mar 11, 2024
71205-531-3030 TABLET in 1 BOTTLE (71205-531-30)Feb 3, 2021
71205-531-6060 TABLET in 1 BOTTLE (71205-531-60)Feb 3, 2021
71205-531-9090 TABLET in 1 BOTTLE (71205-531-90)Feb 3, 2021

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