Package 51655-617-26

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-617-26
Digits Only 5165561726
Product NDC 51655-617
Product ID 51655-617_494f1b73-5bac-20fb-e063-6294a90a6428
Description

90 TABLET, FILM COATED in 1 BOTTLE (51655-617-26)

Marketing

Marketing Status
Marketed Since 2022-09-06
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": "494f1b73-5bac-20fb-e063-6294a90a6428", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898719"], "spl_set_id": ["f32d01db-655b-f3d0-e053-2a95a90a04f6"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (51655-617-26)", "package_ndc": "51655-617-26", "marketing_start_date": "20220906"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-617-52)", "package_ndc": "51655-617-52", "marketing_start_date": "20230920"}], "brand_name": "Benazepril Hydrochloride", "product_id": "51655-617_494f1b73-5bac-20fb-e063-6294a90a6428", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "51655-617", "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": "40 mg/1"}], "application_number": "ANDA078212", "marketing_category": "ANDA", "marketing_start_date": "20220906", "listing_expiration_date": "20271231"}