Package 60760-351-90

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-351-90
Digits Only 6076035190
Product NDC 60760-351
Product ID 60760-351_7a023fd2-27a2-300e-e053-2991aa0aa001
Description

90 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-351-90)

Marketing

Marketing Status
Marketed Since 2017-11-15
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": "7a023fd2-27a2-300e-e053-2991aa0aa001", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898687"], "spl_set_id": ["5e96757f-7daa-194f-e053-2991aa0a8f41"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-351-90)", "package_ndc": "60760-351-90", "marketing_start_date": "20171115"}], "brand_name": "Benazepril Hydrochloride", "product_id": "60760-351_7a023fd2-27a2-300e-e053-2991aa0aa001", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "60760-351", "generic_name": "Benazepril Hydrochloride", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}