NDC 30142-611 – Fexofenadine HCl and Pseudoephedrine HCI

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

Human Otc Drug 1 recall

Product NDC30142-611

Product details

Brand name
Fexofenadine HCl and Pseudoephedrine HCI
Generic name
Fexofenadine HCl and Pseudoephedrine HCI
Labeler
The Kroger Co.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA076667
Marketed since
January 15, 2019
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
30142-611-144 BLISTER PACK in 1 CARTON (30142-611-14) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACKJan 15, 2019

Recalls mentioning this NDC

Other Fexofenadine HCl and Pseudoephedrine HCI products