Drugplain

NDC 33342-131-12

Candesartan Cilexetil and Hydrochlorothiazide 16 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 16 mg/1. Manufactured by Macleods Pharmaceuticals Limited.

Key Facts

Brand Name
Candesartan Cilexetil and Hydrochlorothiazide
Generic Name
Candesartan Cilexetil and Hydrochlorothiazide
NDC Code (Package)
33342-131-12
NDC Code (Product)
33342-131
Manufacturer
Macleods Pharmaceuticals Limited
Strength
16 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Application #
ANDA204100
Drug Class
Thiazide Diuretic [EPC]
Marketing Start
03/07/2015

Recall History

No Recall History

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