Package 82868-016-90

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 82868-016-90
Digits Only 8286801690
Product NDC 82868-016
Description

90 TABLET in 1 BOTTLE, PLASTIC (82868-016-90)

Marketing

Marketing Status
Marketed Since 2023-10-06
Brand hydrochlorothiazide
Generic hydrochlorothiazide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46dc98d5-0f86-9490-e063-6394a90a95c0", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["197770"], "spl_set_id": ["076017ce-8aad-1336-e063-6394a90a76b5"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (82868-016-90)", "package_ndc": "82868-016-90", "marketing_start_date": "20231006"}], "brand_name": "HYDROCHLOROTHIAZIDE", "product_id": "82868-016_46dc98d5-0f86-9490-e063-6394a90a95c0", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "82868-016", "generic_name": "hydrochlorothiazide", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA085182", "marketing_category": "ANDA", "marketing_start_date": "20231006", "listing_expiration_date": "20261231"}