Package 70518-4113-0

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 70518-4113-0
Digits Only 7051841130
Product NDC 70518-4113
Product ID 70518-4113_3c554e53-4fe4-5d93-e063-6394a90a1901
Description

30 TABLET in 1 BLISTER PACK (70518-4113-0)

Marketing

Marketing Status
Marketed Since 2024-06-26
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": "3c554e53-4fe4-5d93-e063-6394a90a1901", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["f20fd735-30c7-4f89-8ceb-b6186646eea6"], "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 (70518-4113-0)", "package_ndc": "70518-4113-0", "marketing_start_date": "20240626"}], "brand_name": "Hydrochlorothiazide", "product_id": "70518-4113_3c554e53-4fe4-5d93-e063-6394a90a1901", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "70518-4113", "generic_name": "Hydrochlorothiazide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA087059", "marketing_category": "ANDA", "marketing_start_date": "20240626", "listing_expiration_date": "20261231"}