Package 71205-244-90

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-244-90
Digits Only 7120524490
Product NDC 71205-244
Product ID 71205-244_0a3833b4-573a-486f-84ee-dd1737356353
Description

90 TABLET in 1 BOTTLE (71205-244-90)

Marketing

Marketing Status
Marketed Since 2019-03-01
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": "0a3833b4-573a-486f-84ee-dd1737356353", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898690"], "spl_set_id": ["9593989f-3129-48ad-9b30-f0b52fb3e91e"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-244-30)", "package_ndc": "71205-244-30", "marketing_start_date": "20190301"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-244-60)", "package_ndc": "71205-244-60", "marketing_start_date": "20190301"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-244-90)", "package_ndc": "71205-244-90", "marketing_start_date": "20190301"}], "brand_name": "Benazepril Hydrochloride", "product_id": "71205-244_0a3833b4-573a-486f-84ee-dd1737356353", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "71205-244", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Proficient Rx LP", "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": "20100202", "listing_expiration_date": "20261231"}