Package 50090-3359-0

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-3359-0
Digits Only 5009033590
Product NDC 50090-3359
Product ID 50090-3359_4a6b0e09-3f06-4d54-8ea6-ce8e130f37d8
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-3359-0)

Marketing

Marketing Status
Marketed Since 2018-03-26
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": "4a6b0e09-3f06-4d54-8ea6-ce8e130f37d8", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898719"], "spl_set_id": ["c5090372-41bf-4677-b198-97fd55a0cb87"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-3359-0)", "package_ndc": "50090-3359-0", "marketing_start_date": "20180326"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-3359-1)", "package_ndc": "50090-3359-1", "marketing_start_date": "20180202"}], "brand_name": "Benazepril Hydrochloride", "product_id": "50090-3359_4a6b0e09-3f06-4d54-8ea6-ce8e130f37d8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "50090-3359", "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": "ANDA078212", "marketing_category": "ANDA", "marketing_start_date": "20080522", "listing_expiration_date": "20261231"}