Package 55154-4343-0

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55154-4343-0
Digits Only 5515443430
Product NDC 55154-4343
Description

10 BLISTER PACK in 1 BAG (55154-4343-0) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2014-04-28
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": "f9ad508c-0909-440b-9e04-f8402009a57e", "openfda": {"upc": ["0055154434409", "0055154434300"], "unii": ["N1SN99T69T"], "rxcui": ["898687", "898690"], "spl_set_id": ["f265e6dd-f47e-4511-9468-282184bcd1b1"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-4343-0)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "55154-4343-0", "marketing_start_date": "20140428"}], "brand_name": "Benazepril Hydrochloride", "product_id": "55154-4343_f9ad508c-0909-440b-9e04-f8402009a57e", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "55154-4343", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Cardinal Health 107, LLC", "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": "20140428", "listing_expiration_date": "20261231"}