Package 71335-0854-2

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-0854-2
Digits Only 7133508542
Product NDC 71335-0854
Description

60 TABLET in 1 BOTTLE (71335-0854-2)

Marketing

Marketing Status
Marketed Since 2022-03-09
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": "a518664a-2636-475f-824b-81cc1e710c78", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898687"], "spl_set_id": ["cd1a7c8f-cc61-4ee4-a259-0b3329cced3e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0854-1)", "package_ndc": "71335-0854-1", "marketing_start_date": "20180817"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0854-2)", "package_ndc": "71335-0854-2", "marketing_start_date": "20220309"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-0854-3)", "package_ndc": "71335-0854-3", "marketing_start_date": "20220411"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0854-4)", "package_ndc": "71335-0854-4", "marketing_start_date": "20180611"}], "brand_name": "Benazepril Hydrochloride", "product_id": "71335-0854_a518664a-2636-475f-824b-81cc1e710c78", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "71335-0854", "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": "ANDA076820", "marketing_category": "ANDA", "marketing_start_date": "20100202", "listing_expiration_date": "20261231"}