Package 84386-101-01

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84386-101-01
Digits Only 8438610101
Product NDC 84386-101
Product ID 84386-101_67c64de1-5579-46e4-82ee-c9bbee708e02
Description

100 TABLET, FILM COATED in 1 BOTTLE (84386-101-01)

Marketing

Marketing Status
Marketed Since 2026-01-13
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": "67c64de1-5579-46e4-82ee-c9bbee708e02", "openfda": {"upc": ["0384386101903", "0384386102900", "0384386100906"], "unii": ["N1SN99T69T"], "rxcui": ["898687", "898690", "898719"], "spl_set_id": ["67c64de1-5579-46e4-82ee-c9bbee708e02"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (84386-101-01)", "package_ndc": "84386-101-01", "marketing_start_date": "20260113"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (84386-101-90)", "package_ndc": "84386-101-90", "marketing_start_date": "20260113"}], "brand_name": "Benazepril Hydrochloride", "product_id": "84386-101_67c64de1-5579-46e4-82ee-c9bbee708e02", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "84386-101", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "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": "20260113", "listing_expiration_date": "20271231"}