Package 51655-388-52

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-388-52
Digits Only 5165538852
Product NDC 51655-388
Product ID 51655-388_48fed634-c2b9-ba9e-e063-6394a90aab7b
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-388-52)

Marketing

Marketing Status
Marketed Since 2023-05-19
Brand benazepril hydrochloride
Generic benazepril hydrochloride
Sample Package No

Linked Drug Pages (1)

Benazepril Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "48fed634-c2b9-ba9e-e063-6394a90aab7b", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898690"], "spl_set_id": ["fc4cd253-13ee-9424-e053-6394a90a35a8"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-388-52)", "package_ndc": "51655-388-52", "marketing_start_date": "20230519"}], "brand_name": "Benazepril Hydrochloride", "product_id": "51655-388_48fed634-c2b9-ba9e-e063-6394a90aab7b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "51655-388", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA078212", "marketing_category": "ANDA", "marketing_start_date": "20230519", "listing_expiration_date": "20271231"}