indapamide

Generic: indapamide

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name indapamide
Generic Name indapamide
Labeler direct_rx
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

indapamide 2.5 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-591
Product ID 72189-591_25b5bb79-400e-e266-e063-6394a90abfd8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074299
Listing Expiration 2026-12-31
Marketing Start 2024-10-30

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 72189591
Hyphenated Format 72189-591

Supplemental Identifiers

RxCUI
197816
UNII
F089I0511L
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 indapamide (source: ndc)
Generic Name indapamide (source: ndc)
Application Number ANDA074299 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (72189-591-60)
source: ndc

Packages (1)

Ingredients (1)

indapamide (2.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "25b5bb79-400e-e266-e063-6394a90abfd8", "openfda": {"nui": ["N0000175359", "N0000175420"], "unii": ["F089I0511L"], "rxcui": ["197816"], "spl_set_id": ["25b5bb79-400d-e266-e063-6394a90abfd8"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72189-591-60)", "package_ndc": "72189-591-60", "marketing_start_date": "20241030"}], "brand_name": "Indapamide", "product_id": "72189-591_25b5bb79-400e-e266-e063-6394a90abfd8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]"], "product_ndc": "72189-591", "generic_name": "Indapamide", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Indapamide", "active_ingredients": [{"name": "INDAPAMIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA074299", "marketing_category": "ANDA", "marketing_start_date": "20241030", "listing_expiration_date": "20261231"}