chlorthalidone

Generic: chlorthalidone

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

chlorthalidone 25 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6900
Product ID 0904-6900_7ed40277-0bad-4118-8685-5d3cdc20684f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA089286
Listing Expiration 2026-12-31
Marketing Start 2016-02-12

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 09046900
Hyphenated Format 0904-6900

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 ANDA089286 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (0904-6900-04) / 1 TABLET in 1 BLISTER PACK
  • 100 BLISTER PACK in 1 CARTON (0904-6900-61) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

Ingredients (1)

chlorthalidone (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7ed40277-0bad-4118-8685-5d3cdc20684f", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499"], "spl_set_id": ["2de92cea-8f03-4af0-9d91-d4578510cc53"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-6900-04)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6900-04", "marketing_start_date": "20160212"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6900-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6900-61", "marketing_start_date": "20160212"}], "brand_name": "Chlorthalidone", "product_id": "0904-6900_7ed40277-0bad-4118-8685-5d3cdc20684f", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "0904-6900", "generic_name": "Chlorthalidone", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorthalidone", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "25 mg/1"}], "application_number": "ANDA089286", "marketing_category": "ANDA", "marketing_start_date": "20160212", "listing_expiration_date": "20261231"}