Package 43063-814-01

Brand: lisinopril

Generic: lisinopril
NDC Package

Package Facts

Identity

Package NDC 43063-814-01
Digits Only 4306381401
Product NDC 43063-814
Description

100 TABLET in 1 BOTTLE, PLASTIC (43063-814-01)

Marketing

Marketing Status
Marketed Since 2018-01-05
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": "415b9940-77ea-a174-e063-6294a90a4cfe", "openfda": {"upc": ["0343063810019", "0343063814017", "0343063813010", "0343063812013"], "unii": ["E7199S1YWR"], "rxcui": ["197884", "205326", "311353", "311354", "314076", "314077"], "spl_set_id": ["b62815f3-77fc-4074-a28a-918ab5cc32db"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (43063-814-01)", "package_ndc": "43063-814-01", "marketing_start_date": "20180105"}], "brand_name": "Lisinopril", "product_id": "43063-814_415b9940-77ea-a174-e063-6294a90a4cfe", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "43063-814", "generic_name": "Lisinopril", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "30 mg/1"}], "application_number": "ANDA075743", "marketing_category": "ANDA", "marketing_start_date": "20170830", "listing_expiration_date": "20261231"}