NDC 51316-800 – Fexofenadine Hydrochloride

Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral

Human Otc Drug 1 recall

Product NDC51316-800

Product details

Brand name
Fexofenadine Hydrochloride
Generic name
Fexofenadine Hydrochloride
Labeler
CVS PHARMACY, INC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA091567
Marketed since
September 20, 2022
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 (6)

Package NDCDescriptionSince
51316-800-081 BOTTLE in 1 CARTON (51316-800-08) / 180 TABLET in 1 BOTTLESep 20, 2022
51316-800-151 BLISTER PACK in 1 CARTON (51316-800-15) / 15 TABLET in 1 BLISTER PACKSep 20, 2022
51316-800-301 BOTTLE in 1 CARTON (51316-800-30) / 30 TABLET in 1 BOTTLESep 20, 2022
51316-800-451 BOTTLE in 1 CARTON (51316-800-45) / 45 TABLET in 1 BOTTLESep 20, 2022
51316-800-701 BOTTLE in 1 CARTON (51316-800-70) / 70 TABLET in 1 BOTTLESep 20, 2022
51316-800-901 BOTTLE in 1 CARTON (51316-800-90) / 90 TABLET in 1 BOTTLESep 20, 2022

Recalls mentioning this NDC

Other Fexofenadine Hydrochloride products