Package 72189-591-60

Brand: indapamide

Generic: indapamide
NDC Package

Package Facts

Identity

Package NDC 72189-591-60
Digits Only 7218959160
Product NDC 72189-591
Description

60 TABLET, FILM COATED in 1 BOTTLE (72189-591-60)

Marketing

Marketing Status
Marketed Since 2024-10-30
Brand indapamide
Generic indapamide
Sample Package No

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"}