NDC 33342-131 – Candesartan Cilexetil and Hydrochlorothiazide

Candesartan Cilexetil 16 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC33342-131

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
33342-131-1090 TABLET in 1 BOTTLE (33342-131-10)Mar 7, 2015
33342-131-1210 BLISTER PACK in 1 CARTON (33342-131-12) / 10 TABLET in 1 BLISTER PACKMar 7, 2015
33342-131-15500 TABLET in 1 BOTTLE (33342-131-15)Mar 7, 2015
33342-131-51300 TABLET in 1 BOTTLE (33342-131-51)Mar 7, 2015

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