NDC 69842-052 – Fexofenadine Hydrochloride

Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC69842-052

Product details

Brand name
Fexofenadine Hydrochloride
Generic name
Fexofenadine hydrochloride
Labeler
CVS Health Corp.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076502
Marketed since
April 1, 2011
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 (7)

Package NDCDescriptionSince
69842-052-153 BLISTER PACK in 1 CARTON (69842-052-15) / 5 TABLET in 1 BLISTER PACKApr 1, 2011
69842-052-181 CARTON in 1 CARTON (69842-052-18) / 180 TABLET in 1 CARTONFeb 1, 2013
69842-052-293 BLISTER PACK in 1 CARTON (69842-052-29) / 15 TABLET in 1 BLISTER PACKApr 1, 2011
69842-052-301 BOTTLE in 1 CARTON (69842-052-30) / 30 TABLET in 1 BOTTLEApr 1, 2011
69842-052-451 BOTTLE in 1 CARTON (69842-052-45) / 45 TABLET in 1 BOTTLEApr 1, 2011
69842-052-701 BOTTLE in 1 CARTON (69842-052-70) / 70 TABLET in 1 BOTTLEJan 11, 2019
69842-052-901 BOTTLE in 1 CARTON (69842-052-90) / 90 TABLET in 1 BOTTLEApr 1, 2011

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