atenolol and chlorthalidone (29300-400)

Drug Facts

Product Profile

Brand Name atenolol and chlorthalidone

Generic Name atenolol and chlorthalidone

Labeler unichem pharmaceuticals (usa), inc.

Dosage Form TABLET

Routes

ORAL

Active Ingredients

atenolol 50 mg/1, chlorthalidone 25 mg/1

Manufacturer

Unichem Pharmaceuticals (USA), Inc.

Identifiers & Regulatory

Product NDC 29300-400

Product ID 29300-400_383b2bb2-513e-4bcf-8fc7-32c0cda3481e

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA213302

Listing Expiration 2026-12-31

Marketing Start 2020-11-25

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 29300400

Hyphenated Format 29300-400

Supplemental Identifiers

RxCUI

197382 197383

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 ANDA213302 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

50 mg/1
25 mg/1

source: ndc

Packaging

100 TABLET in 1 BOTTLE (29300-400-01)
500 TABLET in 1 BOTTLE (29300-400-05)

source: ndc

Packages (2)

29300-400-01 100 TABLET in 1 BOTTLE (29300-400-01) 29300-400-05 500 TABLET in 1 BOTTLE (29300-400-05)

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": "383b2bb2-513e-4bcf-8fc7-32c0cda3481e", "openfda": {"nui": ["N0000175359", "N0000175420", "N0000000161", "N0000175556"], "unii": ["Q0MQD1073Q", "50VV3VW0TI"], "rxcui": ["197382", "197383"], "spl_set_id": ["a85d28c1-e812-4c12-aa67-136bff3610e5"], "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": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (29300-400-01)", "package_ndc": "29300-400-01", "marketing_start_date": "20201214"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (29300-400-05)", "package_ndc": "29300-400-05", "marketing_start_date": "20201214"}], "brand_name": "Atenolol and Chlorthalidone", "product_id": "29300-400_383b2bb2-513e-4bcf-8fc7-32c0cda3481e", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "29300-400", "generic_name": "Atenolol and Chlorthalidone", "labeler_name": "Unichem Pharmaceuticals (USA), 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": "ANDA213302", "marketing_category": "ANDA", "marketing_start_date": "20201125", "listing_expiration_date": "20261231"}