NDC 71335-2165 – Fexofenadine hcl

Fexofenadine Hydrochloride 60 mg/1 · Tablet, Film Coated · Oral

Human Otc Drug

Product NDC71335-2165

Product details

Brand name
Fexofenadine hcl
Generic name
Fexofenadine hcl
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204507
Marketed since
August 26, 2021
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 (7)

Package NDCDescriptionSince
71335-2165-130 TABLET, FILM COATED in 1 BOTTLE (71335-2165-1)Sep 6, 2024
71335-2165-210 TABLET, FILM COATED in 1 BOTTLE (71335-2165-2)Aug 25, 2022
71335-2165-360 TABLET, FILM COATED in 1 BOTTLE (71335-2165-3)Sep 6, 2024
71335-2165-490 TABLET, FILM COATED in 1 BOTTLE (71335-2165-4)Sep 6, 2024
71335-2165-514 TABLET, FILM COATED in 1 BOTTLE (71335-2165-5)Sep 6, 2024
71335-2165-620 TABLET, FILM COATED in 1 BOTTLE (71335-2165-6)Sep 6, 2024
71335-2165-712 TABLET, FILM COATED in 1 BOTTLE (71335-2165-7)Nov 8, 2022

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