chlorthalidone

Generic: chlorthalidone

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorthalidone
Generic Name chlorthalidone
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

chlorthalidone 25 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-317
Product ID 60687-317_437e4b1a-b0d4-115d-e063-6394a90a9f94
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA089286
Listing Expiration 2026-12-31
Marketing Start 2017-08-10

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 60687317
Hyphenated Format 60687-317

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 ANDA089286 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-317-01) / 1 TABLET in 1 BLISTER PACK (60687-317-11)
  • 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-317-25) / 1 TABLET in 1 BLISTER PACK (60687-317-95)
source: ndc

Packages (2)

Ingredients (1)

chlorthalidone (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "437e4b1a-b0d4-115d-e063-6394a90a9f94", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499"], "spl_set_id": ["b1ff748d-36e9-4327-aa8a-e8fb22a9d637"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-317-01)  / 1 TABLET in 1 BLISTER PACK (60687-317-11)", "package_ndc": "60687-317-01", "marketing_start_date": "20200720"}, {"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-317-25)  / 1 TABLET in 1 BLISTER PACK (60687-317-95)", "package_ndc": "60687-317-25", "marketing_start_date": "20170810"}], "brand_name": "Chlorthalidone", "product_id": "60687-317_437e4b1a-b0d4-115d-e063-6394a90a9f94", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "60687-317", "generic_name": "Chlorthalidone", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorthalidone", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "25 mg/1"}], "application_number": "ANDA089286", "marketing_category": "ANDA", "marketing_start_date": "20170810", "listing_expiration_date": "20261231"}