Drugplain

Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride 60 mg/1

Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride · TABLET, FILM COATED, EXTENDED RELEASE · KROGER COMPANY

No Recall History
Plain English

Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride is a tablet, film coated, extended release containing fexofenadine hydrochloride and pseudoephedrine hydrochloride at 60 mg/1, taken oral. Manufactured by KROGER COMPANY.

Key Facts

Brand Name
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Generic Name
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
NDC Code (Product)
30142-059
Manufacturer
KROGER COMPANY
Strength
60 mg/1
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Marketing Status
Application #
ANDA209116
Marketing Start
03/15/2021

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

product quality issue8 reports
drug ineffective7 reports
dizziness4 reports
extra dose administered4 reports
headache4 reports
nausea4 reports
chest discomfort2 reports
constipation2 reports
diarrhoea2 reports
malaise2 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies reduces swelling of nasal passages temporarily relieves sinus congestion and pressure temporarily restores freer breathing through the nose

Dosage & Administration

Directions do not divide, crush, chew or dissolve the tablet; swallow tablet whole adults and children 12 years of age and over take 1 tablet with a glass of water every 12 hours on an empty stomach; do not take more than 2 tablets in 24 hours children under 12 years of age do not use adults 65 years of age and older ask a doctor consumers with kidney disease ask a doctor

Warnings

Warnings

Frequently Asked Questions

What is Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride used for?

Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride contains Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride. It is a tablet, film coated, extended release taken oral. Consult your doctor for specific uses.

Is Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride a controlled substance?

Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride is not classified as a controlled substance by the DEA.

What is the generic name for Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride?

The generic name for Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride is Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride. There are 1 other brand versions of Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride.

What is the NDC code for Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride 60 mg/1?

The NDC (National Drug Code) for Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride 60 mg/1 is 30142-059, listed by KROGER COMPANY.

Product NDC

30142-059

Package NDC

30142-059-20

Other Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Dosages

Other Fexofenadine Brands

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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)