Package 65862-116-01

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 65862-116-01
Digits Only 6586211601
Product NDC 65862-116
Product ID 65862-116_65334c7f-e49f-44d9-a6c1-6c1ce6e88fbe
Description

100 TABLET, FILM COATED in 1 BOTTLE (65862-116-01)

Marketing

Marketing Status
Marketed Since 2008-05-22
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": "65334c7f-e49f-44d9-a6c1-6c1ce6e88fbe", "openfda": {"upc": ["0365862117908", "0365862118905", "0365862116901"], "unii": ["N1SN99T69T"], "rxcui": ["898687", "898690", "898719"], "spl_set_id": ["09e383a8-e912-4cf7-8fb3-05545af80dd0"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-116-01)", "package_ndc": "65862-116-01", "marketing_start_date": "20080522"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-116-90)", "package_ndc": "65862-116-90", "marketing_start_date": "20080522"}], "brand_name": "Benazepril Hydrochloride", "product_id": "65862-116_65334c7f-e49f-44d9-a6c1-6c1ce6e88fbe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "65862-116", "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": "10 mg/1"}], "application_number": "ANDA078212", "marketing_category": "ANDA", "marketing_start_date": "20080522", "listing_expiration_date": "20261231"}