chlorthalidone
Generic: chlorthalidone
Labeler: avpakDrug Facts
Product Profile
Brand Name
chlorthalidone
Generic Name
chlorthalidone
Labeler
avpak
Dosage Form
TABLET
Routes
Active Ingredients
chlorthalidone 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50268-167
Product ID
50268-167_4ba86077-8f44-68da-e063-6294a90ac2ff
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210742
Listing Expiration
2027-12-31
Marketing Start
2019-11-12
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50268167
Hyphenated Format
50268-167
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
- 25 mg/1
Packaging
- 50 BLISTER PACK in 1 BOX (50268-167-15) / 1 TABLET in 1 BLISTER PACK (50268-167-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ba86077-8f44-68da-e063-6294a90ac2ff", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499"], "spl_set_id": ["972b801e-c4f2-4bd6-e053-2a95a90a53bb"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-167-15) / 1 TABLET in 1 BLISTER PACK (50268-167-11)", "package_ndc": "50268-167-15", "marketing_start_date": "20191112"}], "brand_name": "CHLORTHALIDONE", "product_id": "50268-167_4ba86077-8f44-68da-e063-6294a90ac2ff", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "50268-167", "generic_name": "CHLORTHALIDONE", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORTHALIDONE", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "25 mg/1"}], "application_number": "ANDA210742", "marketing_category": "ANDA", "marketing_start_date": "20191112", "listing_expiration_date": "20271231"}