Package 43063-748-30

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-748-30
Digits Only 4306374830
Product NDC 43063-748
Product ID 43063-748_414b5f6d-0d07-7d47-e063-6394a90a496a
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-748-30)

Marketing

Marketing Status
Marketed Since 2017-02-24
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": "414b5f6d-0d07-7d47-e063-6394a90a496a", "openfda": {"upc": ["0343063748305"], "unii": ["N1SN99T69T"], "rxcui": ["898719"], "spl_set_id": ["5de2ea54-877d-46e9-b4c2-bf1ab9d0f19c"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-748-30)", "package_ndc": "43063-748-30", "marketing_start_date": "20170224"}], "brand_name": "Benazepril Hydrochloride", "product_id": "43063-748_414b5f6d-0d07-7d47-e063-6394a90a496a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "43063-748", "generic_name": "Benazepril Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA078212", "marketing_category": "ANDA", "marketing_start_date": "20080522", "listing_expiration_date": "20261231"}