Package 68071-1775-1

Brand: lisinopril

Generic: lisinopril
NDC Package

Package Facts

Identity

Package NDC 68071-1775-1
Digits Only 6807117751
Product NDC 68071-1775
Product ID 68071-1775_1d517b0b-16d8-162e-e063-6394a90a91d0
Description

100 TABLET in 1 BOTTLE (68071-1775-1)

Marketing

Marketing Status
Marketed Since 2017-08-24
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": "1d517b0b-16d8-162e-e063-6394a90a91d0", "openfda": {"upc": ["0368071177510"], "unii": ["E7199S1YWR"], "rxcui": ["314077"], "spl_set_id": ["5786b8d9-3818-66a5-e053-2991aa0a7025"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-1775-1)", "package_ndc": "68071-1775-1", "marketing_start_date": "20170824"}], "brand_name": "LISINOPRIL", "product_id": "68071-1775_1d517b0b-16d8-162e-e063-6394a90a91d0", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "68071-1775", "generic_name": "Lisinopril", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LISINOPRIL", "active_ingredients": [{"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "ANDA076164", "marketing_category": "ANDA", "marketing_start_date": "20111101", "listing_expiration_date": "20261231"}