chlorthalidone

Generic: chlorthalidone

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorthalidone
Generic Name chlorthalidone
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

chlorthalidone 25 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 55289-067
Product ID 55289-067_4198ea35-1b74-f175-e063-6294a90a412e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA086831
Listing Expiration 2026-12-31
Marketing Start 1981-02-26

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 55289067
Hyphenated Format 55289-067

Supplemental Identifiers

RxCUI
197499
UPC
0355289067306
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 ANDA086831 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (55289-067-30)
source: ndc

Packages (1)

55289-067-30 30 TABLET in 1 BOTTLE, PLASTIC (55289-067-30)

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": "4198ea35-1b74-f175-e063-6294a90a412e", "openfda": {"nui": ["N0000175359", "N0000175420"], "upc": ["0355289067306"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499"], "spl_set_id": ["bb7112ae-3a37-4525-8c7f-c0f4100ffc0a"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (55289-067-30)", "package_ndc": "55289-067-30", "marketing_start_date": "20160317"}], "brand_name": "Chlorthalidone", "product_id": "55289-067_4198ea35-1b74-f175-e063-6294a90a412e", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "55289-067", "generic_name": "chlorthalidone", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorthalidone", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "25 mg/1"}], "application_number": "ANDA086831", "marketing_category": "ANDA", "marketing_start_date": "19810226", "listing_expiration_date": "20261231"}