Package 51655-674-52

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 51655-674-52
Digits Only 5165567452
Product NDC 51655-674
Product ID 51655-674_494f9ca1-cfd0-7457-e063-6394a90a91a3
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-674-52)

Marketing

Marketing Status
Marketed Since 2023-02-27
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": "494f9ca1-cfd0-7457-e063-6394a90a91a3", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["429503"], "spl_set_id": ["f331769a-ff11-6c68-e053-2a95a90a493b"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-674-26)", "package_ndc": "51655-674-26", "marketing_start_date": "20230108"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-674-52)", "package_ndc": "51655-674-52", "marketing_start_date": "20230227"}], "brand_name": "HYDROCHLOROTHIAZIDE", "product_id": "51655-674_494f9ca1-cfd0-7457-e063-6394a90a91a3", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "51655-674", "generic_name": "HYDROCHLOROTHIAZIDE", "labeler_name": "Northwind Health Company, LLC", "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": "20230108", "listing_expiration_date": "20271231"}