atenolol and chlorthalidone

Generic: atenolol and chlorthalidone

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atenolol and chlorthalidone
Generic Name atenolol and chlorthalidone
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atenolol 50 mg/1, chlorthalidone 25 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 55289-993
Product ID 55289-993_419b8a9a-2ee9-ef30-e063-6294a90a3e94
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)
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 55289993
Hyphenated Format 55289-993

Supplemental Identifiers

RxCUI
197383
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 ANDA073665 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (55289-993-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (55289-993-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (55289-993-90)
source: ndc

Packages (3)

55289-993-30 30 TABLET in 1 BOTTLE, PLASTIC (55289-993-30) 55289-993-60 60 TABLET in 1 BOTTLE, PLASTIC (55289-993-60) 55289-993-90 90 TABLET in 1 BOTTLE, PLASTIC (55289-993-90)

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": "419b8a9a-2ee9-ef30-e063-6294a90a3e94", "openfda": {"nui": ["N0000000161", "N0000175556", "N0000175359", "N0000175420"], "unii": ["50VV3VW0TI", "Q0MQD1073Q"], "rxcui": ["197383"], "spl_set_id": ["78b374f8-0e16-4c15-85c1-16609ac3aca2"], "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": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (55289-993-30)", "package_ndc": "55289-993-30", "marketing_start_date": "19960424"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (55289-993-60)", "package_ndc": "55289-993-60", "marketing_start_date": "20000508"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (55289-993-90)", "package_ndc": "55289-993-90", "marketing_start_date": "20090518"}], "brand_name": "Atenolol and Chlorthalidone", "product_id": "55289-993_419b8a9a-2ee9-ef30-e063-6294a90a3e94", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "55289-993", "generic_name": "Atenolol and Chlorthalidone", "labeler_name": "PD-Rx Pharmaceuticals, 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"}