Package 70518-4251-0

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 70518-4251-0
Digits Only 7051842510
Product NDC 70518-4251
Product ID 70518-4251_48be1916-5399-8ece-e063-6394a90abba3
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-4251-0)

Marketing

Marketing Status
Marketed Since 2025-01-07
Brand hydrochlorothiazide
Generic hydrochlorothiazide
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "48be1916-5399-8ece-e063-6394a90abba3", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["429503"], "spl_set_id": ["686a5743-adc9-4729-9dbf-5cbc2c23897a"], "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 (70518-4251-0)", "package_ndc": "70518-4251-0", "marketing_start_date": "20250107"}], "brand_name": "HYDROCHLOROTHIAZIDE", "product_id": "70518-4251_48be1916-5399-8ece-e063-6394a90abba3", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "70518-4251", "generic_name": "hydrochlorothiazide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA085182", "marketing_category": "ANDA", "marketing_start_date": "20250107", "listing_expiration_date": "20271231"}