chlorthalidone

Generic: chlorthalidone

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorthalidone
Generic Name chlorthalidone
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

chlorthalidone 25 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-592
Product ID 71205-592_0befef0b-102e-4d9b-b451-6ef769a54f2b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207222
Listing Expiration 2026-12-31
Marketing Start 2018-05-28

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 71205592
Hyphenated Format 71205-592

Supplemental Identifiers

RxCUI
197499
UPC
0371205592301
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 ANDA207222 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71205-592-30)
  • 60 TABLET in 1 BOTTLE (71205-592-60)
  • 90 TABLET in 1 BOTTLE (71205-592-90)
source: ndc

Packages (3)

71205-592-30 30 TABLET in 1 BOTTLE (71205-592-30) 71205-592-60 60 TABLET in 1 BOTTLE (71205-592-60) 71205-592-90 90 TABLET in 1 BOTTLE (71205-592-90)

Ingredients (1)

chlorthalidone (25 mg/1)

Linked Drug Pages (1)

Chlorthalidone ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0befef0b-102e-4d9b-b451-6ef769a54f2b", "openfda": {"nui": ["N0000175359", "N0000175420"], "upc": ["0371205592301"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499"], "spl_set_id": ["01337f79-4b3d-4749-a82b-8d56c1aec179"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-592-30)", "package_ndc": "71205-592-30", "marketing_start_date": "20210721"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-592-60)", "package_ndc": "71205-592-60", "marketing_start_date": "20210721"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-592-90)", "package_ndc": "71205-592-90", "marketing_start_date": "20210721"}], "brand_name": "Chlorthalidone", "product_id": "71205-592_0befef0b-102e-4d9b-b451-6ef769a54f2b", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "71205-592", "generic_name": "Chlorthalidone", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorthalidone", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "25 mg/1"}], "application_number": "ANDA207222", "marketing_category": "ANDA", "marketing_start_date": "20180528", "listing_expiration_date": "20261231"}