chlorthalidone
Generic: chlorthalidone
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
chlorthalidone
Generic Name
chlorthalidone
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
chlorthalidone 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-5183
Product ID
50090-5183_2563551e-9a87-4767-8a2a-db8ba242e7e6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213412
Listing Expiration
2027-12-31
Marketing Start
2020-02-13
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500905183
Hyphenated Format
50090-5183
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
ANDA213412 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (50090-5183-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2563551e-9a87-4767-8a2a-db8ba242e7e6", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["Q0MQD1073Q"], "rxcui": ["197500"], "spl_set_id": ["583992c2-b789-4267-9a8f-c1ee5db3f29f"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5183-1)", "package_ndc": "50090-5183-1", "marketing_start_date": "20200928"}], "brand_name": "Chlorthalidone", "product_id": "50090-5183_2563551e-9a87-4767-8a2a-db8ba242e7e6", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "50090-5183", "generic_name": "Chlorthalidone", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorthalidone", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "50 mg/1"}], "application_number": "ANDA213412", "marketing_category": "ANDA", "marketing_start_date": "20200213", "listing_expiration_date": "20271231"}