Package 51655-202-26

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-202-26
Digits Only 5165520226
Product NDC 51655-202
Product ID 51655-202_48d289fe-098c-d402-e063-6394a90a8036
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-202-26)

Marketing

Marketing Status
Marketed Since 2023-03-15
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": "48d289fe-098c-d402-e063-6394a90a8036", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898687"], "spl_set_id": ["f7f9dc46-a947-7ae3-e053-6394a90a1192"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-202-26)", "package_ndc": "51655-202-26", "marketing_start_date": "20230315"}], "brand_name": "Benazepril Hydrochloride", "product_id": "51655-202_48d289fe-098c-d402-e063-6394a90a8036", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "51655-202", "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": "10 mg/1"}], "application_number": "ANDA078212", "marketing_category": "ANDA", "marketing_start_date": "20230315", "listing_expiration_date": "20271231"}