Package 50228-111-10

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 50228-111-10
Digits Only 5022811110
Product NDC 50228-111
Product ID 50228-111_5c6f4c6a-cc43-4f4d-bc16-688310c98c72
Description

1000 TABLET in 1 BOTTLE (50228-111-10)

Marketing

Marketing Status
Marketed Since 2014-07-23
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": "5c6f4c6a-cc43-4f4d-bc16-688310c98c72", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0350228111300", "0350228111102", "0350228112109"], "unii": ["0J48LPH2TH"], "rxcui": ["197770", "310798"], "spl_set_id": ["02e96a51-1d56-460c-8c20-3d6f37e0ce46"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["ScieGen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (50228-111-10)", "package_ndc": "50228-111-10", "marketing_start_date": "20140723"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50228-111-30)", "package_ndc": "50228-111-30", "marketing_start_date": "20140723"}], "brand_name": "Hydrochlorothiazide", "product_id": "50228-111_5c6f4c6a-cc43-4f4d-bc16-688310c98c72", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "50228-111", "generic_name": "Hydrochlorothiazide", "labeler_name": "ScieGen Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA203018", "marketing_category": "ANDA", "marketing_start_date": "20140723", "listing_expiration_date": "20261231"}