NDC 70771-1326 – Candesartan cilexetil and hydrochlorothiazide

Candesartan Cilexetil 32 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70771-1326

Product details

Brand name
Candesartan cilexetil and hydrochlorothiazide
Generic name
Candesartan cilexetil and hydrochlorothiazide
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203466
Marketed since
April 14, 2018
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker; Thiazide Diuretic

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
70771-1326-01000 TABLET in 1 BOTTLE (70771-1326-0)Apr 14, 2018
70771-1326-1100 TABLET in 1 BOTTLE (70771-1326-1)Apr 14, 2018
70771-1326-330 TABLET in 1 BOTTLE (70771-1326-3)Apr 14, 2018
70771-1326-410 BLISTER PACK in 1 CARTON (70771-1326-4) / 10 TABLET in 1 BLISTER PACK (70771-1326-2)Apr 14, 2018
70771-1326-990 TABLET in 1 BOTTLE (70771-1326-9)Apr 14, 2018

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