Package 42708-165-30

Brand: lisinopril

Generic: lisinopril
NDC Package Sample

Package Facts

Identity

Package NDC 42708-165-30
Digits Only 4270816530
Product NDC 42708-165
Product ID 42708-165_4681a929-3969-1024-e063-6394a90a0935
Description

30 TABLET in 1 BOTTLE, PLASTIC (42708-165-30)

Marketing

Marketing Status
Marketed Since 2023-03-15
Brand lisinopril
Generic lisinopril
Sample Package Yes

Linked Drug Pages (1)

Lisinopril ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4681a929-3969-1024-e063-6394a90a0935", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["314077"], "spl_set_id": ["f6f68322-f8a1-9011-e053-6394a90a1d2c"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET in 1 BOTTLE, PLASTIC (42708-165-30)", "package_ndc": "42708-165-30", "marketing_start_date": "20230315"}], "brand_name": "Lisinopril", "product_id": "42708-165_4681a929-3969-1024-e063-6394a90a0935", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "42708-165", "generic_name": "Lisinopril", "labeler_name": "QPharma, Inc.", "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": "20170512", "listing_expiration_date": "20261231"}