chlorthalidone

Generic: chlorthalidone

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

Drug Facts

Product Profile

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

chlorthalidone 50 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-359
Product ID 72789-359_2bece570-2ffe-8b23-e063-6294a90a525b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA089286
Listing Expiration 2026-12-31
Marketing Start 2023-10-27

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 72789359
Hyphenated Format 72789-359

Supplemental Identifiers

RxCUI
197499 197500
UPC
0372789359304
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 ANDA089286 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-359-30)
  • 90 TABLET in 1 BOTTLE, PLASTIC (72789-359-90)
source: ndc

Packages (2)

Ingredients (1)

chlorthalidone (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2bece570-2ffe-8b23-e063-6294a90a525b", "openfda": {"nui": ["N0000175359", "N0000175420"], "upc": ["0372789359304"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499", "197500"], "spl_set_id": ["08b7ee65-53a5-ffbb-e063-6294a90ad4ee"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-359-30)", "package_ndc": "72789-359-30", "marketing_start_date": "20231027"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-359-90)", "package_ndc": "72789-359-90", "marketing_start_date": "20231027"}], "brand_name": "Chlorthalidone", "product_id": "72789-359_2bece570-2ffe-8b23-e063-6294a90a525b", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "72789-359", "generic_name": "Chlorthalidone", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorthalidone", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "50 mg/1"}], "application_number": "ANDA089286", "marketing_category": "ANDA", "marketing_start_date": "20231027", "listing_expiration_date": "20261231"}