Package 71335-0078-6

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-0078-6
Digits Only 7133500786
Product NDC 71335-0078
Description

10 TABLET, COATED in 1 BOTTLE (71335-0078-6)

Marketing

Marketing Status
Marketed Since 2022-02-09
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": "c561231e-6648-43dc-a435-ac40c8b4cc1f", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898690"], "spl_set_id": ["0653322d-70c6-45f7-a9d1-41efee1d7387"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (71335-0078-1)", "package_ndc": "71335-0078-1", "marketing_start_date": "20220209"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (71335-0078-2)", "package_ndc": "71335-0078-2", "marketing_start_date": "20220209"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (71335-0078-3)", "package_ndc": "71335-0078-3", "marketing_start_date": "20220209"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (71335-0078-4)", "package_ndc": "71335-0078-4", "marketing_start_date": "20220209"}, {"sample": false, "description": "14 TABLET, COATED in 1 BOTTLE (71335-0078-5)", "package_ndc": "71335-0078-5", "marketing_start_date": "20220209"}, {"sample": false, "description": "10 TABLET, COATED in 1 BOTTLE (71335-0078-6)", "package_ndc": "71335-0078-6", "marketing_start_date": "20220209"}], "brand_name": "Benazepril Hydrochloride", "product_id": "71335-0078_c561231e-6648-43dc-a435-ac40c8b4cc1f", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "71335-0078", "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": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}