Package 82868-089-30

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82868-089-30
Digits Only 8286808930
Product NDC 82868-089
Product ID 82868-089_471cd311-f328-da25-e063-6294a90a6ab7
Description

30 TABLET, COATED in 1 BOTTLE, PLASTIC (82868-089-30)

Marketing

Marketing Status
Marketed Since 2025-10-02
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": "471cd311-f328-da25-e063-6294a90a6ab7", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898719"], "spl_set_id": ["471cd30a-401a-c8f9-e063-6294a90a4787"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (82868-089-30)", "package_ndc": "82868-089-30", "marketing_start_date": "20251002"}], "brand_name": "Benazepril Hydrochloride", "product_id": "82868-089_471cd311-f328-da25-e063-6294a90a6ab7", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "82868-089", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "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": "20251002", "listing_expiration_date": "20261231"}