Package 72162-1816-3

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1816-3
Digits Only 7216218163
Product NDC 72162-1816
Description

30 TABLET in 1 BOTTLE (72162-1816-3)

Marketing

Marketing Status
Marketed Since 2023-05-08
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": "ea0f1205-c572-429b-ae69-01e6b88a1075", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898687"], "spl_set_id": ["449e89a3-7bef-44eb-8d73-c77ece611cce"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-1816-3)", "package_ndc": "72162-1816-3", "marketing_start_date": "20230508"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72162-1816-9)", "package_ndc": "72162-1816-9", "marketing_start_date": "20230508"}], "brand_name": "Benazepril Hydrochloride", "product_id": "72162-1816_ea0f1205-c572-429b-ae69-01e6b88a1075", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "72162-1816", "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"}