NDC 51660-998 – Fexofenadine Hydrochloride

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

Human Otc Drug 1 recall

Product NDC51660-998

Product details

Brand name
Fexofenadine Hydrochloride
Generic name
Fexofenadine Hydrochloride
Labeler
OHM LABORATORIES INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091567
Marketed since
April 29, 2022
Listing expires
December 31, 2027
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Fexofenadine Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
51660-998-301 BOTTLE in 1 CARTON (51660-998-30) / 30 TABLET, FILM COATED in 1 BOTTLEApr 29, 2022
51660-998-551 BOTTLE in 1 CARTON (51660-998-55) / 150 TABLET, FILM COATED in 1 BOTTLEApr 29, 2022

Recalls mentioning this NDC

Other Fexofenadine Hydrochloride products