Package 67296-1202-9

Brand: lisinopril

Generic: lisinopril
NDC Package

Package Facts

Identity

Package NDC 67296-1202-9
Digits Only 6729612029
Product NDC 67296-1202
Description

90 TABLET in 1 BOTTLE (67296-1202-9)

Marketing

Marketing Status
Marketed Since 2011-11-01
Brand lisinopril
Generic lisinopril
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "490debf7-a097-8582-e063-6394a90a851e", "openfda": {"upc": ["0367296120295"], "unii": ["E7199S1YWR"], "rxcui": ["314077"], "spl_set_id": ["4f08cfc9-7afc-33aa-e054-00144ff88e88"], "manufacturer_name": ["RedPharm Drug, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (67296-1202-3)", "package_ndc": "67296-1202-3", "marketing_start_date": "20111101"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (67296-1202-9)", "package_ndc": "67296-1202-9", "marketing_start_date": "20111101"}], "brand_name": "LISINOPRIL", "product_id": "67296-1202_490debf7-a097-8582-e063-6394a90a851e", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "67296-1202", "generic_name": "LISINOPRIL", "labeler_name": "RedPharm Drug, 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": "20271231"}