chlorthalidone

Generic: chlorthalidone

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorthalidone
Generic Name chlorthalidone
Labeler zydus lifesciences limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

chlorthalidone 50 mg/1

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 70771-1370
Product ID 70771-1370_bd8a63d4-056c-46d9-9e98-4c64cb097f41
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207813
Listing Expiration 2026-12-31
Marketing Start 2019-05-15

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 707711370
Hyphenated Format 70771-1370

Supplemental Identifiers

RxCUI
197499 197500
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 ANDA207813 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (70771-1370-0)
  • 100 TABLET in 1 BOTTLE (70771-1370-1)
source: ndc

Packages (2)

70771-1370-0 1000 TABLET in 1 BOTTLE (70771-1370-0) 70771-1370-1 100 TABLET in 1 BOTTLE (70771-1370-1)

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": "bd8a63d4-056c-46d9-9e98-4c64cb097f41", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["Q0MQD1073Q"], "rxcui": ["197499", "197500"], "spl_set_id": ["6b432c76-b171-4c29-abf4-6d357976e6ef"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (70771-1370-0)", "package_ndc": "70771-1370-0", "marketing_start_date": "20190515"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1370-1)", "package_ndc": "70771-1370-1", "marketing_start_date": "20190515"}], "brand_name": "Chlorthalidone", "product_id": "70771-1370_bd8a63d4-056c-46d9-9e98-4c64cb097f41", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "70771-1370", "generic_name": "Chlorthalidone", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorthalidone", "active_ingredients": [{"name": "CHLORTHALIDONE", "strength": "50 mg/1"}], "application_number": "ANDA207813", "marketing_category": "ANDA", "marketing_start_date": "20190515", "listing_expiration_date": "20261231"}