chlorthalidone
Generic: chlorthalidone
Labeler: northwind health company, llcDrug Facts
Product Profile
Brand Name
chlorthalidone
Generic Name
chlorthalidone
Labeler
northwind health company, llc
Dosage Form
TABLET
Routes
Active Ingredients
chlorthalidone 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51655-477
Product ID
51655-477_490f4355-9be9-f19a-e063-6394a90af240
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210742
Listing Expiration
2027-12-31
Marketing Start
2022-12-02
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51655477
Hyphenated Format
51655-477
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
ANDA210742 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (51655-477-52)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "490f4355-9be9-f19a-e063-6394a90af240", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["Q0MQD1073Q"], "rxcui": ["197500"], "spl_set_id": ["f309b5df-ce39-0d55-e053-2995a90a7878"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-477-52)", "package_ndc": "51655-477-52", "marketing_start_date": "20221202"}], "brand_name": "CHLORTHALIDONE", "product_id": "51655-477_490f4355-9be9-f19a-e063-6394a90af240", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "51655-477", "generic_name": "CHLORTHALIDONE", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORTHALIDONE", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "50 mg/1"}], "application_number": "ANDA210742", "marketing_category": "ANDA", "marketing_start_date": "20221202", "listing_expiration_date": "20271231"}