atacand hct

Generic: candesartan cilexetil and hydrochlorothiazide

Labeler: ani pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name atacand hct
Generic Name candesartan cilexetil and hydrochlorothiazide
Labeler ani pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

candesartan cilexetil 32 mg/1, hydrochlorothiazide 12.5 mg/1

Manufacturer
ANI Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 62559-651
Product ID 62559-651_512f014c-894d-43ff-96a6-1ff05bc476e6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021093
Listing Expiration 2026-12-31
Marketing Start 2018-10-01

Pharmacologic Class

Established (EPC)
thiazide diuretic [epc]
Chemical Structure
thiazides [cs]
Physiologic Effect
increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62559651
Hyphenated Format 62559-651

Supplemental Identifiers

RxCUI
578325 578330 802749 805855 805859 805863
UPC
0362559652902 0362559651905 0362559650908
UNII
0J48LPH2TH R85M2X0D68
NUI
N0000175359 N0000175419 M0471776

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name atacand hct (source: ndc)
Generic Name candesartan cilexetil and hydrochlorothiazide (source: ndc)
Application Number NDA021093 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 32 mg/1
  • 12.5 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (62559-651-90)
source: ndc

Packages (1)

62559-651-90 90 TABLET in 1 BOTTLE (62559-651-90)

Ingredients (2)

candesartan cilexetil (32 mg/1) hydrochlorothiazide (12.5 mg/1)

Linked Drug Pages (1)

ATACAND HCT ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "512f014c-894d-43ff-96a6-1ff05bc476e6", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0362559652902", "0362559651905", "0362559650908"], "unii": ["0J48LPH2TH", "R85M2X0D68"], "rxcui": ["578325", "578330", "802749", "805855", "805859", "805863"], "spl_set_id": ["d91152c4-66ba-466f-b4f9-0da628d42b1d"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62559-651-90)", "package_ndc": "62559-651-90", "marketing_start_date": "20181001"}], "brand_name": "ATACAND HCT", "product_id": "62559-651_512f014c-894d-43ff-96a6-1ff05bc476e6", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "62559-651", "generic_name": "Candesartan Cilexetil and Hydrochlorothiazide", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATACAND HCT", "active_ingredients": [{"name": "CANDESARTAN CILEXETIL", "strength": "32 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "NDA021093", "marketing_category": "NDA", "marketing_start_date": "20181001", "listing_expiration_date": "20261231"}