chlorthalidone
Generic: chlorthalidone
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
chlorthalidone
Generic Name
chlorthalidone
Labeler
major pharmaceuticals
Dosage Form
TABLET
Routes
Active Ingredients
chlorthalidone 25 mg/1
Manufacturer
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)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09046900
Hyphenated Format
0904-6900
Supplemental Identifiers
RxCUI
UNII
NUI
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
source: ndc
Resolved Composition
Strengths
- 25 mg/1
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
Packages (2)
Ingredients (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"}