Package 71335-1086-2
Brand: benazepril hydrochloride
Generic: benazepril hydrochloridePackage Facts
Identity
Package NDC
71335-1086-2
Digits Only
7133510862
Product NDC
71335-1086
Description
60 TABLET in 1 BOTTLE (71335-1086-2)
Marketing
Marketing Status
Brand
benazepril hydrochloride
Generic
benazepril hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fc9d1bd9-f945-7c61-e053-6294a90a3117", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898690"], "spl_set_id": ["2b02c240-4393-48ed-a385-561ced7b7abf"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1086-1)", "package_ndc": "71335-1086-1", "marketing_start_date": "20220504"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1086-2)", "package_ndc": "71335-1086-2", "marketing_start_date": "20220504"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1086-3)", "package_ndc": "71335-1086-3", "marketing_start_date": "20220504"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1086-4)", "package_ndc": "71335-1086-4", "marketing_start_date": "20220504"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (71335-1086-5)", "package_ndc": "71335-1086-5", "marketing_start_date": "20220504"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-1086-6)", "package_ndc": "71335-1086-6", "marketing_start_date": "20220504"}], "brand_name": "Benazepril Hydrochloride", "product_id": "71335-1086_fc9d1bd9-f945-7c61-e053-6294a90a3117", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "71335-1086", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA076820", "marketing_category": "ANDA", "marketing_start_date": "20100202", "listing_expiration_date": "20261231"}