NDC 37808-022 – Fexofenadine HCl and Pseudoephedrine HCI

Fexofenadine Hydrochloride 60 mg/1; Pseudoephedrine Hydrochloride 120 mg/1 · Tablet, Extended Release · Oral

Human Otc Drug

Product NDC37808-022

Product details

Brand name
Fexofenadine HCl and Pseudoephedrine HCI
Generic name
Fexofenadine HCl and Pseudoephedrine HCI
Labeler
HEB
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA076667
Marketed since
December 21, 2015
Listing expires
December 31, 2026
Pharmacologic class
Histamine-1 Receptor Antagonist; alpha-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Fexofenadine HCl and Pseudoephedrine HCI →

Package NDC codes (1)

Package NDCDescriptionSince
37808-022-316 BLISTER PACK in 1 CARTON (37808-022-31) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACKDec 21, 2015

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