Drugplain

NDC 62559-662-90

Candesartan Cilexetil and Hydrochlorothiazide 32 mg/1

Candesartan Cilexetil and Hydrochlorothiazide · TABLET

No Recall History

Candesartan Cilexetil and Hydrochlorothiazide is a tablet containing candesartan cilexetil and hydrochlorothiazide at a strength of 32 mg/1. Manufactured by ANI Pharmaceuticals, Inc..

Key Facts

Brand Name
Candesartan Cilexetil and Hydrochlorothiazide
Generic Name
Candesartan Cilexetil and Hydrochlorothiazide
NDC Code (Package)
62559-662-90
NDC Code (Product)
62559-662
Manufacturer
ANI Pharmaceuticals, Inc.
Strength
32 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Application #
NDA021093
Drug Class
Thiazide Diuretic [EPC]
Marketing Start
09/26/2018

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.