chlorthalidone

Generic: chlorthalidone

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorthalidone
Generic Name chlorthalidone
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

chlorthalidone 25 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2072
Product ID 71335-2072_1e72e940-0c13-4856-9da3-888f33f97b7f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213412
Listing Expiration 2026-12-31
Marketing Start 2020-02-13

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 713352072
Hyphenated Format 71335-2072

Supplemental Identifiers

RxCUI
197499
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 ANDA213412 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-2072-1)
  • 90 TABLET in 1 BOTTLE (71335-2072-2)
  • 60 TABLET in 1 BOTTLE (71335-2072-3)
  • 8 TABLET in 1 BOTTLE (71335-2072-4)
  • 100 TABLET in 1 BOTTLE (71335-2072-5)
source: ndc

Packages (5)

71335-2072-1 30 TABLET in 1 BOTTLE (71335-2072-1) 71335-2072-2 90 TABLET in 1 BOTTLE (71335-2072-2) 71335-2072-3 60 TABLET in 1 BOTTLE (71335-2072-3) 71335-2072-4 8 TABLET in 1 BOTTLE (71335-2072-4) 71335-2072-5 100 TABLET in 1 BOTTLE (71335-2072-5)

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": "1e72e940-0c13-4856-9da3-888f33f97b7f", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499"], "spl_set_id": ["98f4a14c-2863-4068-bd35-aaedcc872680"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2072-1)", "package_ndc": "71335-2072-1", "marketing_start_date": "20220520"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2072-2)", "package_ndc": "71335-2072-2", "marketing_start_date": "20220415"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2072-3)", "package_ndc": "71335-2072-3", "marketing_start_date": "20220916"}, {"sample": false, "description": "8 TABLET in 1 BOTTLE (71335-2072-4)", "package_ndc": "71335-2072-4", "marketing_start_date": "20220916"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2072-5)", "package_ndc": "71335-2072-5", "marketing_start_date": "20220407"}], "brand_name": "Chlorthalidone", "product_id": "71335-2072_1e72e940-0c13-4856-9da3-888f33f97b7f", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "71335-2072", "generic_name": "Chlorthalidone", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorthalidone", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "25 mg/1"}], "application_number": "ANDA213412", "marketing_category": "ANDA", "marketing_start_date": "20200213", "listing_expiration_date": "20261231"}