Package 70518-4466-0

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 70518-4466-0
Digits Only 7051844660
Product NDC 70518-4466
Product ID 70518-4466_4149f0d8-1e41-f7f3-e063-6394a90a0d55
Description

30 TABLET in 1 BLISTER PACK (70518-4466-0)

Marketing

Marketing Status
Marketed Since 2025-09-04
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": "4149f0d8-1e41-f7f3-e063-6394a90a0d55", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["429503"], "spl_set_id": ["71691ccf-0ed9-4a14-8da6-7ab9b9698f52"], "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": "30 TABLET in 1 BLISTER PACK (70518-4466-0)", "package_ndc": "70518-4466-0", "marketing_start_date": "20250904"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4466-1)", "package_ndc": "70518-4466-1", "marketing_start_date": "20251016"}], "brand_name": "HYDROCHLOROTHIAZIDE", "product_id": "70518-4466_4149f0d8-1e41-f7f3-e063-6394a90a0d55", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "70518-4466", "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": "ANDA040702", "marketing_category": "ANDA", "marketing_start_date": "20250904", "listing_expiration_date": "20261231"}