NDC 47335-724-66
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride 60 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 60 mg/1. Manufactured by Sun Pharmaceutical Industries, Inc..
Key Facts
- Brand Name
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
- Generic Name
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
- NDC Code (Package)
47335-724-66- NDC Code (Product)
47335-724- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Strength
- 60 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA090818
- Marketing Start
- 03/01/2018
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.