Package 51655-335-26

Brand: lisinopril

Generic: lisinopril
NDC Package

Package Facts

Identity

Package NDC 51655-335-26
Digits Only 5165533526
Product NDC 51655-335
Description

90 TABLET in 1 BOTTLE, PLASTIC (51655-335-26)

Marketing

Marketing Status
Marketed Since 2020-05-21
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": "48eb0bba-4c41-73b4-e063-6294a90a7a83", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["197884"], "spl_set_id": ["ab2f8ab5-3c87-484a-e053-2995a90a42bb"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-335-26)", "package_ndc": "51655-335-26", "marketing_start_date": "20200521"}], "brand_name": "LISINOPRIL", "product_id": "51655-335_48eb0bba-4c41-73b4-e063-6294a90a7a83", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "51655-335", "generic_name": "Lisinopril", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LISINOPRIL", "active_ingredients": [{"name": "LISINOPRIL", "strength": "40 mg/1"}], "application_number": "ANDA076164", "marketing_category": "ANDA", "marketing_start_date": "20200521", "listing_expiration_date": "20271231"}