chlorthalidone

Generic: chlorthalidone

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorthalidone
Generic Name chlorthalidone
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

chlorthalidone 50 mg/1

Manufacturer
Northwind Health Company, LLC

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)
thiazide-like diuretic [epc]
Physiologic Effect
increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655477
Hyphenated Format 51655-477

Supplemental Identifiers

RxCUI
197500
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 ANDA210742 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (51655-477-52)
source: ndc

Packages (1)

Ingredients (1)

chlorthalidone (50 mg/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"}