NDC 41415-995-30
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride 60 mg/1
fexofenadine hydrochloride and pseudoephedrine hydrochloride · TABLET, EXTENDED RELEASE
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride is a tablet, extended release containing fexofenadine hydrochloride and pseudoephedrine hydrochloride at a strength of 60 mg/1. Manufactured by PUBLIX SUPER MARKETS, INC.
Key Facts
- Brand Name
- Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
- Generic Name
- fexofenadine hydrochloride and pseudoephedrine hydrochloride
- NDC Code (Package)
41415-995-30- NDC Code (Product)
41415-995- Manufacturer
- PUBLIX SUPER MARKETS, INC
- Strength
- 60 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA090818
- Marketing Start
- 11/08/2021
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.