Package 68645-532-54

Brand: lisinopril

Generic: lisinopril
NDC Package

Package Facts

Identity

Package NDC 68645-532-54
Digits Only 6864553254
Product NDC 68645-532
Product ID 68645-532_4742db84-1ab9-25f5-e063-6394a90a1859
Description

30 TABLET in 1 BOTTLE (68645-532-54)

Marketing

Marketing Status
Marketed Since 2017-03-07
Brand lisinopril
Generic lisinopril
Sample Package No

Linked Drug Pages (1)

Lisinopril ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4742db84-1ab9-25f5-e063-6394a90a1859", "openfda": {"upc": ["0368645532547"], "unii": ["E7199S1YWR"], "rxcui": ["314077"], "spl_set_id": ["2688aa37-1ab9-4353-8689-8c2347ec5d3c"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68645-532-54)", "package_ndc": "68645-532-54", "marketing_start_date": "20170307"}], "brand_name": "Lisinopril", "product_id": "68645-532_4742db84-1ab9-25f5-e063-6394a90a1859", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "68645-532", "generic_name": "Lisinopril", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "ANDA077321", "marketing_category": "ANDA", "marketing_start_date": "20170307", "listing_expiration_date": "20261231"}