Package 72189-110-30

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72189-110-30
Digits Only 7218911030
Product NDC 72189-110
Product ID 72189-110_2be8edce-01da-2a51-e063-6294a90ac7d7
Description

30 TABLET, COATED in 1 BOTTLE (72189-110-30)

Marketing

Marketing Status
Marketed Since 2020-06-12
Brand benazepril hydrochloride
Generic benazepril hydrochloride
Sample Package No

Linked Drug Pages (1)

BENAZEPRIL HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2be8edce-01da-2a51-e063-6294a90ac7d7", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898687"], "spl_set_id": ["a7e4e43a-7abc-e2a5-e053-2995a90ab5f4"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (72189-110-30)", "package_ndc": "72189-110-30", "marketing_start_date": "20200612"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (72189-110-90)", "package_ndc": "72189-110-90", "marketing_start_date": "20200612"}], "brand_name": "BENAZEPRIL HYDROCHLORIDE", "product_id": "72189-110_2be8edce-01da-2a51-e063-6294a90ac7d7", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "72189-110", "generic_name": "BENAZEPRIL HYDROCHLORIDE", "labeler_name": "DIRECT RX", "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": "20200612", "listing_expiration_date": "20261231"}