Package 68645-557-54

Brand: lisinopril and hydrochlorothiazide

Generic: lisinopril and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 68645-557-54
Digits Only 6864555754
Product NDC 68645-557
Description

30 TABLET in 1 BOTTLE (68645-557-54)

Marketing

Marketing Status
Marketed Since 2006-04-10
Brand lisinopril and hydrochlorothiazide
Generic lisinopril and hydrochlorothiazide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4c4ae743-258c-e380-e063-6394a90af48a", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0368645556543", "0368645557540", "0368645558547"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197885", "197886", "197887"], "spl_set_id": ["6d729ec5-7311-4534-9999-9d6fa4f3ba2f"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68645-557-54)", "package_ndc": "68645-557-54", "marketing_start_date": "20060410"}], "brand_name": "Lisinopril and Hydrochlorothiazide", "product_id": "68645-557_4c4ae743-258c-e380-e063-6394a90af48a", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "68645-557", "generic_name": "Lisinopril and Hydrochlorothiazide", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "ANDA077912", "marketing_category": "ANDA", "marketing_start_date": "20060410", "listing_expiration_date": "20271231"}