Package 71205-320-90

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-320-90
Digits Only 7120532090
Product NDC 71205-320
Product ID 71205-320_63cc7078-2579-49df-8a10-8d5b3b8c169b
Description

90 TABLET, FILM COATED in 1 BOTTLE (71205-320-90)

Marketing

Marketing Status
Marketed Since 2019-09-01
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": "63cc7078-2579-49df-8a10-8d5b3b8c169b", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898719"], "spl_set_id": ["92a26516-3d84-4d7a-a770-523926507887"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-320-30)", "package_ndc": "71205-320-30", "marketing_start_date": "20190901"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-320-60)", "package_ndc": "71205-320-60", "marketing_start_date": "20190901"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-320-90)", "package_ndc": "71205-320-90", "marketing_start_date": "20190901"}], "brand_name": "Benazepril Hydrochloride", "product_id": "71205-320_63cc7078-2579-49df-8a10-8d5b3b8c169b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "71205-320", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Proficient Rx LP", "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": "20080522", "listing_expiration_date": "20261231"}