NDC 58602-844-60
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride 180 mg/1
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride · TABLET, FILM COATED, EXTENDED RELEASE
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride is a tablet, film coated, extended release containing fexofenadine hydrochloride and pseudoephedrine hydrochloride at a strength of 180 mg/1. Manufactured by Aurohealth LLC.
Key Facts
- Brand Name
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
- Generic Name
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
- NDC Code (Package)
58602-844-60- NDC Code (Product)
58602-844- Manufacturer
- Aurohealth LLC
- Strength
- 180 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA215232
- Marketing Start
- 04/17/2025
Recall History
No Recall HistoryView Full Drug Page
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.