Package 72789-303-01

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 72789-303-01
Digits Only 7278930301
Product NDC 72789-303
Product ID 72789-303_3cf6edf5-e1bb-570f-e063-6294a90af580
Description

100 TABLET in 1 BOTTLE, PLASTIC (72789-303-01)

Marketing

Marketing Status
Marketed Since 2022-03-02
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": "3cf6edf5-e1bb-570f-e063-6294a90af580", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0372789303017"], "unii": ["0J48LPH2TH"], "rxcui": ["197770"], "spl_set_id": ["67bedecc-f758-4bc6-82c5-7d428cbbbd9b"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-303-01)", "package_ndc": "72789-303-01", "marketing_start_date": "20220302"}], "brand_name": "Hydrochlorothiazide", "product_id": "72789-303_3cf6edf5-e1bb-570f-e063-6294a90af580", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "72789-303", "generic_name": "Hydrochlorothiazide", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "20080815", "listing_expiration_date": "20261231"}