chlorthalidone

Generic: chlorthalidone

Labeler: ascend laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorthalidone
Generic Name chlorthalidone
Labeler ascend laboratories, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

chlorthalidone 25 mg/1

Manufacturer
Ascend Laboratories, LLC

Identifiers & Regulatory

Product NDC 67877-696
Product ID 67877-696_c8bc4f9d-d8fe-47fa-8643-95a371c5d23b
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 67877696
Hyphenated Format 67877-696

Supplemental Identifiers

RxCUI
197499 197500
UNII
Q0MQD1073Q
NUI
N0000175359 N0000175420

Packaging Origin

Original Packager
true

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
  • 100 TABLET in 1 BOTTLE (67877-696-01)
  • 1000 TABLET in 1 BOTTLE (67877-696-10)
  • 1 BLISTER PACK in 1 CARTON (67877-696-33) / 10 TABLET in 1 BLISTER PACK
  • 10 BLISTER PACK in 1 CARTON (67877-696-38) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (4)

67877-696-01 100 TABLET in 1 BOTTLE (67877-696-01) 67877-696-10 1000 TABLET in 1 BOTTLE (67877-696-10) 67877-696-33 1 BLISTER PACK in 1 CARTON (67877-696-33) / 10 TABLET in 1 BLISTER PACK 67877-696-38 10 BLISTER PACK in 1 CARTON (67877-696-38) / 10 TABLET in 1 BLISTER PACK

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": "c8bc4f9d-d8fe-47fa-8643-95a371c5d23b", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499", "197500"], "spl_set_id": ["d104583e-e983-4230-b6d1-4455ee1060a5"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (67877-696-01)", "package_ndc": "67877-696-01", "marketing_start_date": "20200213"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (67877-696-10)", "package_ndc": "67877-696-10", "marketing_start_date": "20200213"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (67877-696-33)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "67877-696-33", "marketing_start_date": "20200213"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (67877-696-38)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "67877-696-38", "marketing_start_date": "20200213"}], "brand_name": "Chlorthalidone", "product_id": "67877-696_c8bc4f9d-d8fe-47fa-8643-95a371c5d23b", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "67877-696", "generic_name": "Chlorthalidone", "labeler_name": "Ascend Laboratories, LLC", "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"}