Package 30698-449-01

Brand: lotensin

Generic: benazepril hydrochloride
NDC Package

Package Facts

Identity

Package NDC 30698-449-01
Digits Only 3069844901
Product NDC 30698-449
Product ID 30698-449_40029d07-adfa-0cc3-e063-6294a90a4cd5
Description

100 TABLET in 1 BOTTLE (30698-449-01)

Marketing

Marketing Status
Marketed Since 1991-06-21
Brand lotensin
Generic benazepril hydrochloride
Sample Package No

Linked Drug Pages (1)

Lotensin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40029d07-adfa-0cc3-e063-6294a90a4cd5", "openfda": {"upc": ["0330698449011"], "unii": ["N1SN99T69T"], "rxcui": ["898687", "898689", "898690", "898692", "898719", "898721"], "spl_set_id": ["2abb091b-a53e-46b0-9b84-e5ee8f2bdd8e"], "manufacturer_name": ["Validus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (30698-449-01)", "package_ndc": "30698-449-01", "marketing_start_date": "19910621"}], "brand_name": "Lotensin", "product_id": "30698-449_40029d07-adfa-0cc3-e063-6294a90a4cd5", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "30698-449", "generic_name": "benazepril hydrochloride", "labeler_name": "Validus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lotensin", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "NDA019851", "marketing_category": "NDA", "marketing_start_date": "19910621", "listing_expiration_date": "20261231"}