Package 72189-513-90

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 72189-513-90
Digits Only 7218951390
Product NDC 72189-513
Product ID 72189-513_2c4e72a3-e1c7-eee1-e063-6294a90a89bb
Description

90 TABLET in 1 BOTTLE (72189-513-90)

Marketing

Marketing Status
Marketed Since 2023-09-11
Brand hydrochlorothiazide
Generic hydrochlorothiazide
Sample Package No

Linked Drug Pages (1)

Hydrochlorothiazide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4e72a3-e1c7-eee1-e063-6294a90a89bb", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["197770"], "spl_set_id": ["05156717-fe1b-22f1-e063-6394a90a3d10"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-513-90)", "package_ndc": "72189-513-90", "marketing_start_date": "20230911"}], "brand_name": "Hydrochlorothiazide", "product_id": "72189-513_2c4e72a3-e1c7-eee1-e063-6294a90a89bb", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "72189-513", "generic_name": "Hydrochlorothiazide", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA040907", "marketing_category": "ANDA", "marketing_start_date": "20230911", "listing_expiration_date": "20261231"}