Package 63187-393-30

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63187-393-30
Digits Only 6318739330
Product NDC 63187-393
Description

30 TABLET, COATED in 1 BOTTLE (63187-393-30)

Marketing

Marketing Status
Marketed Since 2016-09-01
Brand benazepril hydrochloride
Generic benazepril hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cac335b0-2fc0-420f-b52a-a7216e940192", "openfda": {"upc": ["0363187393908"], "unii": ["N1SN99T69T"], "rxcui": ["898690"], "spl_set_id": ["be41d21c-4747-47bb-b4b7-bbfabcd7a9b1"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (63187-393-30)", "package_ndc": "63187-393-30", "marketing_start_date": "20160901"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (63187-393-90)", "package_ndc": "63187-393-90", "marketing_start_date": "20160901"}], "brand_name": "Benazepril Hydrochloride", "product_id": "63187-393_cac335b0-2fc0-420f-b52a-a7216e940192", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "63187-393", "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": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}