NDC 68196-107 – Fexofenadine Hydrochloride

Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC68196-107

Product details

Brand name
Fexofenadine Hydrochloride
Generic name
Fexofenadine hydrochloride
Labeler
Sam's West Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076502
Marketed since
May 9, 2017
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 (2)

Package NDCDescriptionSince
68196-107-151 BOTTLE in 1 CARTON (68196-107-15) / 150 TABLET in 1 BOTTLEMay 9, 2017
68196-107-50150 TABLET in 1 BOTTLE (68196-107-50)Apr 1, 2023

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