NDC 68788-7449 – Fexofenadine HCL

Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC68788-7449

Product details

Brand name
Fexofenadine HCL
Generic name
Fexofenadine HCL
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204097
Marketed since
August 19, 2016
Listing expires
December 31, 2027
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
68788-7449-1100 TABLET in 1 BOTTLE (68788-7449-1)Dec 27, 2019
68788-7449-330 TABLET in 1 BOTTLE (68788-7449-3)Dec 27, 2019
68788-7449-660 TABLET in 1 BOTTLE (68788-7449-6)Dec 27, 2019
68788-7449-990 TABLET in 1 BOTTLE (68788-7449-9)Dec 27, 2019

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