Package 50268-111-15

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-111-15
Digits Only 5026811115
Product NDC 50268-111
Description

50 BLISTER PACK in 1 BOX (50268-111-15) / 1 TABLET in 1 BLISTER PACK (50268-111-11)

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": "3f7e3955-e107-517a-e063-6294a90a0b13", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898687", "898690", "898719", "898723"], "spl_set_id": ["f004d7e2-fc45-8a37-e548-eeaaa327f9b5"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-111-15)  / 1 TABLET in 1 BLISTER PACK (50268-111-11)", "package_ndc": "50268-111-15", "marketing_start_date": "20140428"}], "brand_name": "Benazepril Hydrochloride", "product_id": "50268-111_3f7e3955-e107-517a-e063-6294a90a0b13", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "50268-111", "generic_name": "Benazepril Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA076820", "marketing_category": "ANDA", "marketing_start_date": "20140428", "listing_expiration_date": "20261231"}