Package 70839-300-30

Brand: tekturna

Generic: aliskiren hemifumarate
NDC Package

Package Facts

Identity

Package NDC 70839-300-30
Digits Only 7083930030
Product NDC 70839-300
Product ID 70839-300_130d24ec-4b3b-0978-e063-6394a90af0c8
Description

30 TABLET, FILM COATED in 1 BOTTLE (70839-300-30)

Marketing

Marketing Status
Marketed Since 2017-01-01
Brand tekturna
Generic aliskiren hemifumarate
Sample Package No

Linked Drug Pages (1)

Tekturna ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "130d24ec-4b3b-0978-e063-6394a90af0c8", "openfda": {"upc": ["0370839300306"], "unii": ["C8A0P8G029"], "rxcui": ["1011736", "1011738", "1011739", "1011741"], "spl_set_id": ["3dd61fa5-1620-4ebf-bbdb-ede29b92fce2"], "manufacturer_name": ["LXO US Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70839-300-30)", "package_ndc": "70839-300-30", "marketing_start_date": "20170101"}], "brand_name": "Tekturna", "product_id": "70839-300_130d24ec-4b3b-0978-e063-6394a90af0c8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Renin Inhibitor [EPC]", "Renin Inhibitors [MoA]"], "product_ndc": "70839-300", "generic_name": "aliskiren hemifumarate", "labeler_name": "LXO US Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tekturna", "active_ingredients": [{"name": "ALISKIREN HEMIFUMARATE", "strength": "300 mg/1"}], "application_number": "NDA021985", "marketing_category": "NDA", "marketing_start_date": "20070305", "listing_expiration_date": "20261231"}