Package 70518-2125-0

Brand: benazepril hydrochloride

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2125-0
Digits Only 7051821250
Product NDC 70518-2125
Product ID 70518-2125_49a0827c-f0bd-2aa2-e063-6394a90abb0a
Description

90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2125-0)

Marketing

Marketing Status
Marketed Since 2019-05-31
Brand benazepril hydrochloride
Generic benazepril hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49a0827c-f0bd-2aa2-e063-6394a90abb0a", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898719"], "spl_set_id": ["afd616b9-0c75-48be-862d-5ac18364fd9d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2125-0)", "package_ndc": "70518-2125-0", "marketing_start_date": "20190531"}], "brand_name": "Benazepril Hydrochloride", "product_id": "70518-2125_49a0827c-f0bd-2aa2-e063-6394a90abb0a", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "70518-2125", "generic_name": "Benazepril Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "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": "20190531", "listing_expiration_date": "20271231"}