Package 71335-0457-2
Brand: benazepril hydrochloride
Generic: benazepril hydrochloridePackage Facts
Identity
Package NDC
71335-0457-2
Digits Only
7133504572
Product NDC
71335-0457
Description
60 TABLET, COATED in 1 BOTTLE (71335-0457-2)
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": "9b7748b4-9ef6-4dbd-9589-916d87c9e991", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898687"], "spl_set_id": ["b0d3122a-5332-4af6-98d8-520ed70ace62"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (71335-0457-1)", "package_ndc": "71335-0457-1", "marketing_start_date": "20220209"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (71335-0457-2)", "package_ndc": "71335-0457-2", "marketing_start_date": "20220209"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (71335-0457-3)", "package_ndc": "71335-0457-3", "marketing_start_date": "20220209"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (71335-0457-4)", "package_ndc": "71335-0457-4", "marketing_start_date": "20220209"}], "brand_name": "Benazepril Hydrochloride", "product_id": "71335-0457_9b7748b4-9ef6-4dbd-9589-916d87c9e991", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "71335-0457", "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": "10 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}