Package 50268-110-15
Brand: benazepril hydrochloride
Generic: benazepril hydrochloridePackage Facts
Identity
Package NDC
50268-110-15
Digits Only
5026811015
Product NDC
50268-110
Description
50 BLISTER PACK in 1 BOX (50268-110-15) / 1 TABLET in 1 BLISTER PACK (50268-110-11)
Marketing
Marketing Status
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 (50268-110-15) / 1 TABLET in 1 BLISTER PACK (50268-110-11)", "package_ndc": "50268-110-15", "marketing_start_date": "20140428"}], "brand_name": "Benazepril Hydrochloride", "product_id": "50268-110_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": "50268-110", "generic_name": "Benazepril Hydrochloride", "labeler_name": "AvPAK", "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"}