chlorthalidone

Generic: chlorthalidone

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorthalidone
Generic Name chlorthalidone
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

chlorthalidone 25 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-356
Product ID 72189-356_2c4c9187-3303-d75f-e063-6394a90a9231
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211627
Listing Expiration 2026-12-31
Marketing Start 2022-05-10

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 72189356
Hyphenated Format 72189-356

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 ANDA211627 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (72189-356-60)
source: ndc

Packages (1)

72189-356-60 60 TABLET in 1 BOTTLE (72189-356-60)

Ingredients (1)

chlorthalidone (25 mg/1)

Linked Drug Pages (1)

Chlorthalidone ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4c9187-3303-d75f-e063-6394a90a9231", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499"], "spl_set_id": ["deab1d3e-759f-480e-e053-2995a90a0a75"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-356-60)", "package_ndc": "72189-356-60", "marketing_start_date": "20220510"}], "brand_name": "Chlorthalidone", "product_id": "72189-356_2c4c9187-3303-d75f-e063-6394a90a9231", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "72189-356", "generic_name": "Chlorthalidone", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorthalidone", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "25 mg/1"}], "application_number": "ANDA211627", "marketing_category": "ANDA", "marketing_start_date": "20220510", "listing_expiration_date": "20261231"}