Package 51655-341-26

Brand: enalapril maleate

Generic: enalapril maleate
NDC Package

Package Facts

Identity

Package NDC 51655-341-26
Digits Only 5165534126
Product NDC 51655-341
Description

90 TABLET in 1 BOTTLE, PLASTIC (51655-341-26)

Marketing

Marketing Status
Marketed Since 2020-05-28
Brand enalapril maleate
Generic enalapril maleate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48eb2d46-5438-a385-e063-6294a90a0fc7", "openfda": {"unii": ["9O25354EPJ"], "rxcui": ["858810"], "spl_set_id": ["ab2ffb6e-4628-e44c-e053-2a95a90a2336"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-341-26)", "package_ndc": "51655-341-26", "marketing_start_date": "20200528"}], "brand_name": "Enalapril Maleate", "product_id": "51655-341_48eb2d46-5438-a385-e063-6294a90a0fc7", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "51655-341", "generic_name": "Enalapril Maleate", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril Maleate", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "20 mg/1"}], "application_number": "ANDA075657", "marketing_category": "ANDA", "marketing_start_date": "20200528", "listing_expiration_date": "20271231"}