Package 68071-1672-1

Brand: lisinopril

Generic: lisinopril
NDC Package

Package Facts

Identity

Package NDC 68071-1672-1
Digits Only 6807116721
Product NDC 68071-1672
Product ID 68071-1672_1d4e3508-f3b0-3203-e063-6294a90addb1
Description

100 TABLET in 1 BOTTLE (68071-1672-1)

Marketing

Marketing Status
Marketed Since 2017-09-26
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": "1d4e3508-f3b0-3203-e063-6294a90addb1", "openfda": {"upc": ["0368071167214"], "unii": ["E7199S1YWR"], "rxcui": ["314076"], "spl_set_id": ["5a1c5b04-b78c-c057-e053-2991aa0aa916"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-1672-1)", "package_ndc": "68071-1672-1", "marketing_start_date": "20170926"}], "brand_name": "LISINOPRIL", "product_id": "68071-1672_1d4e3508-f3b0-3203-e063-6294a90addb1", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "68071-1672", "generic_name": "Lisinopril", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LISINOPRIL", "active_ingredients": [{"name": "LISINOPRIL", "strength": "10 mg/1"}], "application_number": "ANDA076180", "marketing_category": "ANDA", "marketing_start_date": "20111101", "listing_expiration_date": "20261231"}