Package 67296-2043-3

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 67296-2043-3
Digits Only 6729620433
Product NDC 67296-2043
Description

30 TABLET in 1 BOTTLE (67296-2043-3)

Marketing

Marketing Status
Marketed Since 2009-07-02
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": "2c6315d7-bf5f-5845-e063-6394a90ab261", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0329300129014", "0329300128017"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["fa1c0b92-4360-bcfd-e053-6394a90a955a"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Redpharm drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (67296-2043-3)", "package_ndc": "67296-2043-3", "marketing_start_date": "20090702"}], "brand_name": "Hydrochlorothiazide", "product_id": "67296-2043_2c6315d7-bf5f-5845-e063-6394a90ab261", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "67296-2043", "generic_name": "Hydrochlorothiazide", "labeler_name": "Redpharm drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA040907", "marketing_category": "ANDA", "marketing_start_date": "20080815", "listing_expiration_date": "20261231"}