Package 72789-101-01

Brand: lisinopril

Generic: lisinopril
NDC Package

Package Facts

Identity

Package NDC 72789-101-01
Digits Only 7278910101
Product NDC 72789-101
Description

100 TABLET in 1 BOTTLE, PLASTIC (72789-101-01)

Marketing

Marketing Status
Marketed Since 2020-07-15
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": "4031d438-4492-8f2e-e063-6394a90a9510", "openfda": {"upc": ["0372789101019"], "unii": ["E7199S1YWR"], "rxcui": ["311353"], "spl_set_id": ["705582ed-da8c-418f-8bb2-fc0b74ed0a88"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-101-01)", "package_ndc": "72789-101-01", "marketing_start_date": "20200715"}], "brand_name": "LISINOPRIL", "product_id": "72789-101_4031d438-4492-8f2e-e063-6394a90a9510", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "72789-101", "generic_name": "Lisinopril", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LISINOPRIL", "active_ingredients": [{"name": "LISINOPRIL", "strength": "2.5 mg/1"}], "application_number": "ANDA076164", "marketing_category": "ANDA", "marketing_start_date": "20111101", "listing_expiration_date": "20261231"}