Package 72162-1356-0

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 72162-1356-0
Digits Only 7216213560
Product NDC 72162-1356
Product ID 72162-1356_050d39a9-6f11-4374-be7b-b2b82fca3e49
Description

1000 TABLET in 1 BOTTLE, PLASTIC (72162-1356-0)

Marketing

Marketing Status
Marketed Since 2023-10-04
Brand hydrochlorothiazide
Generic hydrochlorothiazide
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "050d39a9-6f11-4374-be7b-b2b82fca3e49", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["1b47bf17-8a09-4728-985d-d466d6a83a0c"], "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": "1000 TABLET in 1 BOTTLE, PLASTIC (72162-1356-0)", "package_ndc": "72162-1356-0", "marketing_start_date": "20231004"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72162-1356-1)", "package_ndc": "72162-1356-1", "marketing_start_date": "20231004"}], "brand_name": "Hydrochlorothiazide", "product_id": "72162-1356_050d39a9-6f11-4374-be7b-b2b82fca3e49", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "72162-1356", "generic_name": "Hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA040412", "marketing_category": "ANDA", "marketing_start_date": "20020329", "listing_expiration_date": "20261231"}