NDC 70677-1009 – Fexofenadine Hydrochloride

Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC70677-1009

Product details

Brand name
Fexofenadine Hydrochloride
Generic name
Fexofenadine hydrochloride
Labeler
Strategic Sourcing Services, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076502
Marketed since
September 9, 2019
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 (3)

Package NDCDescriptionSince
70677-1009-13 BLISTER PACK in 1 CARTON (70677-1009-1) / 5 TABLET in 1 BLISTER PACKMay 5, 2023
70677-1009-21 BOTTLE in 1 CARTON (70677-1009-2) / 30 TABLET in 1 BOTTLEMay 5, 2023
70677-1009-31 BOTTLE in 1 CARTON (70677-1009-3) / 70 TABLET in 1 BOTTLEMay 5, 2023

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