Package 63187-499-30

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63187-499-30
Digits Only 6318749930
Product NDC 63187-499
Product ID 63187-499_8b462d0b-fe6e-4240-abd2-2eafbf58a98d
Description

30 TABLET, COATED in 1 BOTTLE (63187-499-30)

Marketing

Marketing Status
Marketed Since 2015-02-02
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": "8b462d0b-fe6e-4240-abd2-2eafbf58a98d", "openfda": {"upc": ["0363187500306", "0363187499907"], "unii": ["N1SN99T69T"], "rxcui": ["898687", "898723"], "spl_set_id": ["ebdf5144-752d-456f-b46d-19cbba0bc3d7"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (63187-499-30)", "package_ndc": "63187-499-30", "marketing_start_date": "20150202"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (63187-499-60)", "package_ndc": "63187-499-60", "marketing_start_date": "20150202"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (63187-499-90)", "package_ndc": "63187-499-90", "marketing_start_date": "20150202"}], "brand_name": "Benazepril Hydrochloride", "product_id": "63187-499_8b462d0b-fe6e-4240-abd2-2eafbf58a98d", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "63187-499", "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": "10 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}