Package 62135-721-90

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-721-90
Digits Only 6213572190
Product NDC 62135-721
Product ID 62135-721_24246e61-c66b-9c3e-e063-6294a90a5207
Description

90 TABLET in 1 BOTTLE (62135-721-90)

Marketing

Marketing Status
Marketed Since 2023-07-20
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": "24246e61-c66b-9c3e-e063-6294a90a5207", "openfda": {"upc": ["0362135721909", "0362135720902", "0362135719906", "0362135722906"], "unii": ["N1SN99T69T"], "rxcui": ["898687", "898690", "898719", "898723"], "spl_set_id": ["df13d8d8-0d70-4d6f-9dd1-5da38fbe2562"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-721-90)", "package_ndc": "62135-721-90", "marketing_start_date": "20230720"}], "brand_name": "Benazepril hydrochloride", "product_id": "62135-721_24246e61-c66b-9c3e-e063-6294a90a5207", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "62135-721", "generic_name": "Benazepril hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA076267", "marketing_category": "ANDA", "marketing_start_date": "20220820", "listing_expiration_date": "20261231"}