Package 72162-1357-1

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 72162-1357-1
Digits Only 7216213571
Product NDC 72162-1357
Product ID 72162-1357_2f36dc8e-b15a-4945-b8d9-25c98f5ba66b
Description

100 TABLET in 1 BOTTLE, PLASTIC (72162-1357-1)

Marketing

Marketing Status
Marketed Since 2024-02-05
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": "2f36dc8e-b15a-4945-b8d9-25c98f5ba66b", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["197770"], "spl_set_id": ["78d65a02-c78e-4f98-b756-3cb5ee78f252"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72162-1357-1)", "package_ndc": "72162-1357-1", "marketing_start_date": "20240205"}], "brand_name": "Hydrochlorothiazide", "product_id": "72162-1357_2f36dc8e-b15a-4945-b8d9-25c98f5ba66b", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "72162-1357", "generic_name": "Hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA040412", "marketing_category": "ANDA", "marketing_start_date": "20020329", "listing_expiration_date": "20261231"}