Package 68071-5130-0

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-5130-0
Digits Only 6807151300
Product NDC 68071-5130
Product ID 68071-5130_1b54a8a1-0ece-633c-e063-6394a90a1be2
Description

100 TABLET, COATED in 1 BOTTLE (68071-5130-0)

Marketing

Marketing Status
Marketed Since 2019-12-12
Brand benazepril hydrochloride
Generic benazepril hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1b54a8a1-0ece-633c-e063-6394a90a1be2", "openfda": {"upc": ["0368071513004"], "unii": ["N1SN99T69T"], "rxcui": ["898723"], "spl_set_id": ["9987a842-07a5-635e-e053-2995a90afa32"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (68071-5130-0)", "package_ndc": "68071-5130-0", "marketing_start_date": "20191212"}], "brand_name": "Benazepril Hydrochloride", "product_id": "68071-5130_1b54a8a1-0ece-633c-e063-6394a90a1be2", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "68071-5130", "generic_name": "Benazepril Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}