atenolol and chlorthalidone (0591-5782)

Drug Facts

Product Profile

Brand Name atenolol and chlorthalidone

Generic Name atenolol and chlorthalidone

Labeler actavis pharma, inc.

Dosage Form TABLET

Routes

ORAL

Active Ingredients

atenolol 50 mg/1, chlorthalidone 25 mg/1

Manufacturer

Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 0591-5782

Product ID 0591-5782_b15eb43d-d93a-4e5f-b113-bc256779a40d

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA073665

Listing Expiration 2026-12-31

Marketing Start 1992-08-01

Pharmacologic Class

Established (EPC)

thiazide-like diuretic [epc] beta-adrenergic blocker [epc]

Mechanism of Action

adrenergic beta-antagonists [moa]

Physiologic Effect

increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05915782

Hyphenated Format 0591-5782

Supplemental Identifiers

RxCUI

197382 197383

UPC

0305915782011

UNII

Q0MQD1073Q 50VV3VW0TI

NUI

N0000175359 N0000175420 N0000000161 N0000175556

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 atenolol and chlorthalidone (source: ndc)

Generic Name atenolol and chlorthalidone (source: ndc)

Application Number ANDA073665 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

50 mg/1
25 mg/1

source: ndc

Packaging

100 TABLET in 1 BOTTLE (0591-5782-01)

source: ndc

Packages (1)

0591-5782-01 100 TABLET in 1 BOTTLE (0591-5782-01)

Ingredients (2)

atenolol (50 mg/1) chlorthalidone (25 mg/1)

Linked Drug Pages (1)

Atenolol and Chlorthalidone ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "b15eb43d-d93a-4e5f-b113-bc256779a40d", "openfda": {"nui": ["N0000175359", "N0000175420", "N0000000161", "N0000175556"], "upc": ["0305915782011"], "unii": ["Q0MQD1073Q", "50VV3VW0TI"], "rxcui": ["197382", "197383"], "spl_set_id": ["a6794dfa-adbb-491b-9d48-f89a44e866c5"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]", "beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0591-5782-01)", "package_ndc": "0591-5782-01", "marketing_start_date": "19920801"}], "brand_name": "Atenolol and Chlorthalidone", "product_id": "0591-5782_b15eb43d-d93a-4e5f-b113-bc256779a40d", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0591-5782", "generic_name": "Atenolol and Chlorthalidone", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atenolol and Chlorthalidone", "active_ingredients": [{"name": "ATENOLOL", "strength": "50 mg/1"}, {"name": "CHLORTHALIDONE", "strength": "25 mg/1"}], "application_number": "ANDA073665", "marketing_category": "ANDA", "marketing_start_date": "19920801", "listing_expiration_date": "20261231"}