atenolol and chlorthalidone (70518-4111)

Drug Facts

Product Profile

Brand Name atenolol and chlorthalidone

Generic Name atenolol and chlorthalidone

Labeler remedyrepack inc.

Dosage Form TABLET

Routes

ORAL

Active Ingredients

atenolol 100 mg/1, chlorthalidone 25 mg/1

Manufacturer

REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4111

Product ID 70518-4111_3fa50d1a-a2d5-8e11-e063-6294a90a3bbc

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA213302

Listing Expiration 2026-12-31

Marketing Start 2024-06-25

Pharmacologic Class

Established (EPC)

beta-adrenergic blocker [epc] thiazide-like diuretic [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 705184111

Hyphenated Format 70518-4111

Supplemental Identifiers

RxCUI

197382

UNII

50VV3VW0TI Q0MQD1073Q

NUI

N0000000161 N0000175556 N0000175359 N0000175420

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 ANDA213302 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

100 mg/1
25 mg/1

source: ndc

Packaging

90 TABLET in 1 BOTTLE, PLASTIC (70518-4111-0)

source: ndc

Packages (1)

70518-4111-0 90 TABLET in 1 BOTTLE, PLASTIC (70518-4111-0)

Ingredients (2)

atenolol (100 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": "3fa50d1a-a2d5-8e11-e063-6294a90a3bbc", "openfda": {"nui": ["N0000000161", "N0000175556", "N0000175359", "N0000175420"], "unii": ["50VV3VW0TI", "Q0MQD1073Q"], "rxcui": ["197382"], "spl_set_id": ["dfbd0160-f56a-41b9-a4ff-eb2df73b1e9b"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]", "Thiazide-like Diuretic [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4111-0)", "package_ndc": "70518-4111-0", "marketing_start_date": "20240625"}], "brand_name": "Atenolol and Chlorthalidone", "product_id": "70518-4111_3fa50d1a-a2d5-8e11-e063-6294a90a3bbc", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-4111", "generic_name": "Atenolol and Chlorthalidone", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atenolol and Chlorthalidone", "active_ingredients": [{"name": "ATENOLOL", "strength": "100 mg/1"}, {"name": "CHLORTHALIDONE", "strength": "25 mg/1"}], "application_number": "ANDA213302", "marketing_category": "ANDA", "marketing_start_date": "20240625", "listing_expiration_date": "20261231"}