chlorthalidone

Generic: chlorthalidone

Labeler: dr. reddy's laboratories inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorthalidone
Generic Name chlorthalidone
Labeler dr. reddy's laboratories inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

chlorthalidone 25 mg/1

Manufacturer
Dr. Reddy's Laboratories Inc.

Identifiers & Regulatory

Product NDC 43598-170
Product ID 43598-170_bd2e4486-0720-4d09-b4f5-472c4478af0e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210742
Listing Expiration 2026-12-31
Marketing Start 2022-10-20

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 43598170
Hyphenated Format 43598-170

Supplemental Identifiers

RxCUI
197499 197500
UPC
0343598170015 0343598170107 0343598167015
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 ANDA210742 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (43598-170-01)
  • 1000 TABLET in 1 BOTTLE (43598-170-10)
source: ndc

Packages (2)

43598-170-01 100 TABLET in 1 BOTTLE (43598-170-01) 43598-170-10 1000 TABLET in 1 BOTTLE (43598-170-10)

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": "bd2e4486-0720-4d09-b4f5-472c4478af0e", "openfda": {"nui": ["N0000175359", "N0000175420"], "upc": ["0343598170015", "0343598170107", "0343598167015"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499", "197500"], "spl_set_id": ["bd2e4486-0720-4d09-b4f5-472c4478af0e"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (43598-170-01)", "package_ndc": "43598-170-01", "marketing_start_date": "20221020"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (43598-170-10)", "package_ndc": "43598-170-10", "marketing_start_date": "20221020"}], "brand_name": "CHLORTHALIDONE", "product_id": "43598-170_bd2e4486-0720-4d09-b4f5-472c4478af0e", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "43598-170", "generic_name": "CHLORTHALIDONE", "labeler_name": "Dr. Reddy's Laboratories Inc.", "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": "20221020", "listing_expiration_date": "20261231"}