chlorthalidone

Generic: chlorthalidone

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorthalidone
Generic Name chlorthalidone
Labeler avpak
Dosage Form TABLET
Routes
ORAL
Active Ingredients

chlorthalidone 25 mg/1

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-167
Product ID 50268-167_4ba86077-8f44-68da-e063-6294a90ac2ff
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210742
Listing Expiration 2027-12-31
Marketing Start 2019-11-12

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 50268167
Hyphenated Format 50268-167

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 ANDA210742 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 BOX (50268-167-15) / 1 TABLET in 1 BLISTER PACK (50268-167-11)
source: ndc

Packages (1)

Ingredients (1)

chlorthalidone (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ba86077-8f44-68da-e063-6294a90ac2ff", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499"], "spl_set_id": ["972b801e-c4f2-4bd6-e053-2a95a90a53bb"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-167-15)  / 1 TABLET in 1 BLISTER PACK (50268-167-11)", "package_ndc": "50268-167-15", "marketing_start_date": "20191112"}], "brand_name": "CHLORTHALIDONE", "product_id": "50268-167_4ba86077-8f44-68da-e063-6294a90ac2ff", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "50268-167", "generic_name": "CHLORTHALIDONE", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORTHALIDONE", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "25 mg/1"}], "application_number": "ANDA210742", "marketing_category": "ANDA", "marketing_start_date": "20191112", "listing_expiration_date": "20271231"}