chlorthalidone

Generic: chlorthalidone

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorthalidone
Generic Name chlorthalidone
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

chlorthalidone 25 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8294
Product ID 68788-8294_558b4d05-335d-4287-ae74-1ecbdaef7348
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214129
Listing Expiration 2026-12-31
Marketing Start 2022-11-29

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 687888294
Hyphenated Format 68788-8294

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 ANDA214129 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68788-8294-3)
  • 90 TABLET in 1 BOTTLE (68788-8294-9)
source: ndc

Packages (2)

68788-8294-3 30 TABLET in 1 BOTTLE (68788-8294-3) 68788-8294-9 90 TABLET in 1 BOTTLE (68788-8294-9)

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": "558b4d05-335d-4287-ae74-1ecbdaef7348", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499"], "spl_set_id": ["180cc3c7-6ab7-481b-b860-b20d3599e53f"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8294-3)", "package_ndc": "68788-8294-3", "marketing_start_date": "20230420"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8294-9)", "package_ndc": "68788-8294-9", "marketing_start_date": "20221129"}], "brand_name": "Chlorthalidone", "product_id": "68788-8294_558b4d05-335d-4287-ae74-1ecbdaef7348", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "68788-8294", "generic_name": "Chlorthalidone", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorthalidone", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "25 mg/1"}], "application_number": "ANDA214129", "marketing_category": "ANDA", "marketing_start_date": "20221129", "listing_expiration_date": "20261231"}