NDC 10202-229 – Fexofenadine hydrochloride

Fexofenadine Hydrochloride 180 mg/1 · Tablet, Film Coated · Oral

Human Otc Drug

Product NDC10202-229

Product details

Brand name
Fexofenadine hydrochloride
Generic name
Fexofenadine hydrochloride
Labeler
7-eleven
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202039
Marketed since
January 15, 2015
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 (1)

Package NDCDescriptionSince
10202-229-661 BLISTER PACK in 1 CARTON (10202-229-66) / 10 TABLET, FILM COATED in 1 BLISTER PACKJan 15, 2015

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