chlorthalidone

Generic: chlorthalidone

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorthalidone
Generic Name chlorthalidone
Labeler rising pharma holdings, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

chlorthalidone 50 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 64980-600
Product ID 64980-600_6404aaa7-05c8-4f96-a091-3f07248ffbd5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211320
Listing Expiration 2026-12-31
Marketing Start 2024-10-23

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 64980600
Hyphenated Format 64980-600

Supplemental Identifiers

RxCUI
197499 197500
UPC
0364980599108 0364980599016 0364980600019
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 ANDA211320 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (64980-600-01)
source: ndc

Packages (1)

64980-600-01 100 TABLET in 1 BOTTLE (64980-600-01)

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": "6404aaa7-05c8-4f96-a091-3f07248ffbd5", "openfda": {"nui": ["N0000175359", "N0000175420"], "upc": ["0364980599108", "0364980599016", "0364980600019"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499", "197500"], "spl_set_id": ["71b1d074-0521-4cd1-beb5-fedd61f52eca"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (64980-600-01)", "package_ndc": "64980-600-01", "marketing_start_date": "20241023"}], "brand_name": "CHLORTHALIDONE", "product_id": "64980-600_6404aaa7-05c8-4f96-a091-3f07248ffbd5", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "64980-600", "generic_name": "Chlorthalidone", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORTHALIDONE", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "50 mg/1"}], "application_number": "ANDA211320", "marketing_category": "ANDA", "marketing_start_date": "20241023", "listing_expiration_date": "20261231"}