NDC 33342-133 – Candesartan Cilexetil and Hydrochlorothiazide

Candesartan Cilexetil 32 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC33342-133

Product details

Brand name
Candesartan Cilexetil and Hydrochlorothiazide
Generic name
Candesartan Cilexetil and Hydrochlorothiazide
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204100
Marketed since
March 7, 2015
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin 2 Receptor Blocker; Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Candesartan Cilexetil and Hydrochlorothiazide →

Package NDC codes (4)

Package NDCDescriptionSince
33342-133-1090 TABLET in 1 BOTTLE (33342-133-10)Mar 7, 2015
33342-133-1210 BLISTER PACK in 1 CARTON (33342-133-12) / 10 TABLET in 1 BLISTER PACKMar 7, 2015
33342-133-15500 TABLET in 1 BOTTLE (33342-133-15)Mar 7, 2015
33342-133-51300 TABLET in 1 BOTTLE (33342-133-51)Mar 7, 2015

Other Candesartan Cilexetil and Hydrochlorothiazide products