Package 50090-0914-1

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-0914-1
Digits Only 5009009141
Product NDC 50090-0914
Product ID 50090-0914_64205930-0f5b-4b46-840f-2c89c160d998
Description

90 TABLET, COATED in 1 BOTTLE (50090-0914-1)

Marketing

Marketing Status
Marketed Since 2014-11-28
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": "64205930-0f5b-4b46-840f-2c89c160d998", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898719"], "spl_set_id": ["8f46e2c9-9b3b-48d0-a307-9069e3879959"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (50090-0914-0)", "package_ndc": "50090-0914-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (50090-0914-1)", "package_ndc": "50090-0914-1", "marketing_start_date": "20141128"}], "brand_name": "Benazepril Hydrochloride", "product_id": "50090-0914_64205930-0f5b-4b46-840f-2c89c160d998", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "50090-0914", "generic_name": "Benazepril Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}