chlorthalidone

Generic: chlorthalidone

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorthalidone
Generic Name chlorthalidone
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

chlorthalidone 25 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2133
Product ID 72162-2133_3c337abc-75e5-4ad4-b9e1-417b515d3884
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212878
Listing Expiration 2026-12-31
Marketing Start 2022-08-05

Pharmacologic Class

Established (EPC)
thiazide-like diuretic [epc]
Physiologic Effect
increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622133
Hyphenated Format 72162-2133

Supplemental Identifiers

RxCUI
197499
UNII
Q0MQD1073Q
NUI
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 chlorthalidone (source: ndc)
Generic Name chlorthalidone (source: ndc)
Application Number ANDA212878 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (72162-2133-0)
  • 100 TABLET in 1 BOTTLE (72162-2133-1)
  • 30 TABLET in 1 BOTTLE (72162-2133-3)
  • 60 TABLET in 1 BOTTLE (72162-2133-6)
source: ndc

Packages (4)

Ingredients (1)

chlorthalidone (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c337abc-75e5-4ad4-b9e1-417b515d3884", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499"], "spl_set_id": ["bcd2b6f8-533a-4f50-b3e6-80427e6c19ac"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-2133-0)", "package_ndc": "72162-2133-0", "marketing_start_date": "20230919"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2133-1)", "package_ndc": "72162-2133-1", "marketing_start_date": "20230919"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2133-3)", "package_ndc": "72162-2133-3", "marketing_start_date": "20230919"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72162-2133-6)", "package_ndc": "72162-2133-6", "marketing_start_date": "20230919"}], "brand_name": "Chlorthalidone", "product_id": "72162-2133_3c337abc-75e5-4ad4-b9e1-417b515d3884", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "72162-2133", "generic_name": "Chlorthalidone", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorthalidone", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "25 mg/1"}], "application_number": "ANDA212878", "marketing_category": "ANDA", "marketing_start_date": "20220805", "listing_expiration_date": "20261231"}