Package 70518-3780-0

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 70518-3780-0
Digits Only 7051837800
Product NDC 70518-3780
Product ID 70518-3780_348bc808-7a18-4706-e063-6294a90ab7b8
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-3780-0)

Marketing

Marketing Status
Marketed Since 2023-07-09
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": "348bc808-7a18-4706-e063-6294a90ab7b8", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["197770"], "spl_set_id": ["1570f1ad-8372-477f-89c3-8c9ce01e27d1"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-3780-0)", "package_ndc": "70518-3780-0", "marketing_start_date": "20230709"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3780-1)", "package_ndc": "70518-3780-1", "marketing_start_date": "20231208"}], "brand_name": "HYDROCHLOROTHIAZIDE", "product_id": "70518-3780_348bc808-7a18-4706-e063-6294a90ab7b8", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "70518-3780", "generic_name": "hydrochlorothiazide", "labeler_name": "REMEDYREPACK INC.", "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": "20230709", "listing_expiration_date": "20261231"}