chlorthalidone
Generic: chlorthalidone
Labeler: northstar rx llc.Drug Facts
Product Profile
Brand Name
chlorthalidone
Generic Name
chlorthalidone
Labeler
northstar rx llc.
Dosage Form
TABLET
Routes
Active Ingredients
chlorthalidone 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
16714-129
Product ID
16714-129_1a83a458-0a7f-44f1-b805-6288b06a4359
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207813
Listing Expiration
2026-12-31
Marketing Start
2019-11-21
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
16714129
Hyphenated Format
16714-129
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
ANDA207813 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (16714-129-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1a83a458-0a7f-44f1-b805-6288b06a4359", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499", "197500"], "spl_set_id": ["56635d7a-1fff-4d1f-bf2c-def4b1ad8208"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Northstar Rx LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16714-129-01)", "package_ndc": "16714-129-01", "marketing_start_date": "20191121"}], "brand_name": "Chlorthalidone", "product_id": "16714-129_1a83a458-0a7f-44f1-b805-6288b06a4359", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "16714-129", "generic_name": "Chlorthalidone", "labeler_name": "Northstar Rx LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorthalidone", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "50 mg/1"}], "application_number": "ANDA207813", "marketing_category": "ANDA", "marketing_start_date": "20191121", "listing_expiration_date": "20261231"}