chlorthalidone

Generic: chlorthalidone

Labeler: coupler llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

chlorthalidone 50 mg/1

Manufacturer
Coupler LLC

Identifiers & Regulatory

Product NDC 67046-1495
Product ID 67046-1495_2ccc49ea-3f9b-d9bc-e063-6294a90a389e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207204
Listing Expiration 2026-12-31
Marketing Start 2025-01-28

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 670461495
Hyphenated Format 67046-1495

Supplemental Identifiers

RxCUI
197500
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 ANDA207204 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (67046-1495-3)
source: ndc

Packages (1)

67046-1495-3 30 TABLET in 1 BLISTER PACK (67046-1495-3)

Ingredients (1)

chlorthalidone (50 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": "2ccc49ea-3f9b-d9bc-e063-6294a90a389e", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["Q0MQD1073Q"], "rxcui": ["197500"], "spl_set_id": ["2ccc5376-5fb0-dd09-e063-6294a90af563"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1495-3)", "package_ndc": "67046-1495-3", "marketing_start_date": "20250128"}], "brand_name": "Chlorthalidone", "product_id": "67046-1495_2ccc49ea-3f9b-d9bc-e063-6294a90a389e", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "67046-1495", "generic_name": "Chlorthalidone", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorthalidone", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "50 mg/1"}], "application_number": "ANDA207204", "marketing_category": "ANDA", "marketing_start_date": "20250128", "listing_expiration_date": "20261231"}