Package 63187-906-30

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63187-906-30
Digits Only 6318790630
Product NDC 63187-906
Product ID 63187-906_9eeaae93-ac71-4721-98ad-8c7a9231f822
Description

30 TABLET, COATED in 1 BOTTLE (63187-906-30)

Marketing

Marketing Status
Marketed Since 2017-09-01
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": "9eeaae93-ac71-4721-98ad-8c7a9231f822", "openfda": {"upc": ["0363187906900"], "unii": ["N1SN99T69T"], "rxcui": ["898719"], "spl_set_id": ["313225d7-f947-40b3-96d7-289aad300a4a"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (63187-906-30)", "package_ndc": "63187-906-30", "marketing_start_date": "20170901"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (63187-906-60)", "package_ndc": "63187-906-60", "marketing_start_date": "20170901"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (63187-906-90)", "package_ndc": "63187-906-90", "marketing_start_date": "20170901"}], "brand_name": "Benazepril Hydrochloride", "product_id": "63187-906_9eeaae93-ac71-4721-98ad-8c7a9231f822", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "63187-906", "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": "40 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}