chlorthalidone

Generic: chlorthalidone

Labeler: unichem pharmaceuticals (usa), inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorthalidone
Generic Name chlorthalidone
Labeler unichem pharmaceuticals (usa), inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

chlorthalidone 50 mg/1

Manufacturer
Unichem Pharmaceuticals (USA), Inc.

Identifiers & Regulatory

Product NDC 29300-334
Product ID 29300-334_a126115d-3e90-411b-91de-ccde9090e90f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211627
Listing Expiration 2026-12-31
Marketing Start 2019-08-06

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 29300334
Hyphenated Format 29300-334

Supplemental Identifiers

RxCUI
197499 197500
UPC
0329300333015 0329300334012
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 ANDA211627 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (29300-334-01)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (29300-334-10)
source: ndc

Packages (2)

29300-334-01 100 TABLET in 1 BOTTLE, PLASTIC (29300-334-01) 29300-334-10 1000 TABLET in 1 BOTTLE, PLASTIC (29300-334-10)

Ingredients (1)

chlorthalidone (50 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": "a126115d-3e90-411b-91de-ccde9090e90f", "openfda": {"nui": ["N0000175359", "N0000175420"], "upc": ["0329300333015", "0329300334012"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499", "197500"], "spl_set_id": ["01065eda-7515-46bc-b858-a062c3aa35bd"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (29300-334-01)", "package_ndc": "29300-334-01", "marketing_start_date": "20191001"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (29300-334-10)", "package_ndc": "29300-334-10", "marketing_start_date": "20191001"}], "brand_name": "Chlorthalidone", "product_id": "29300-334_a126115d-3e90-411b-91de-ccde9090e90f", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "29300-334", "generic_name": "Chlorthalidone", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorthalidone", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "50 mg/1"}], "application_number": "ANDA211627", "marketing_category": "ANDA", "marketing_start_date": "20190806", "listing_expiration_date": "20261231"}