chlorthalidone

Generic: chlorthalidone

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorthalidone
Generic Name chlorthalidone
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

chlorthalidone 25 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3718
Product ID 70518-3718_3e999418-08e3-ba6e-e063-6394a90a992c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215587
Listing Expiration 2026-12-31
Marketing Start 2023-04-20

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 705183718
Hyphenated Format 70518-3718

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 ANDA215587 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-3718-0)
  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-3718-1)
source: ndc

Packages (2)

70518-3718-0 30 TABLET in 1 BLISTER PACK (70518-3718-0) 70518-3718-1 90 TABLET in 1 BOTTLE, PLASTIC (70518-3718-1)

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": "3e999418-08e3-ba6e-e063-6394a90a992c", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499"], "spl_set_id": ["0baac2aa-06c4-489e-a3f9-fe9d20cf61a2"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3718-0)", "package_ndc": "70518-3718-0", "marketing_start_date": "20230420"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-3718-1)", "package_ndc": "70518-3718-1", "marketing_start_date": "20250912"}], "brand_name": "CHLORTHALIDONE", "product_id": "70518-3718_3e999418-08e3-ba6e-e063-6394a90a992c", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "70518-3718", "generic_name": "chlorthalidone", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORTHALIDONE", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "25 mg/1"}], "application_number": "ANDA215587", "marketing_category": "ANDA", "marketing_start_date": "20230420", "listing_expiration_date": "20261231"}