Package 49884-425-11

Brand: aliskiren

Generic: aliskiren
NDC Package

Package Facts

Identity

Package NDC 49884-425-11
Digits Only 4988442511
Product NDC 49884-425
Product ID 49884-425_6c3a1f0c-dd67-4849-a8b5-a88f85ac5f43
Description

30 TABLET, FILM COATED in 1 BOTTLE (49884-425-11)

Marketing

Marketing Status
Marketed Since 2019-03-25
Brand aliskiren
Generic aliskiren
Sample Package No

Linked Drug Pages (1)

ALISKIREN ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6c3a1f0c-dd67-4849-a8b5-a88f85ac5f43", "openfda": {"unii": ["C8A0P8G029"], "rxcui": ["1011736", "1011739"], "spl_set_id": ["f3fd2503-25ef-4660-a29a-f62c491e28fb"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (49884-425-11)", "package_ndc": "49884-425-11", "marketing_start_date": "20190325"}], "brand_name": "ALISKIREN", "product_id": "49884-425_6c3a1f0c-dd67-4849-a8b5-a88f85ac5f43", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Renin Inhibitor [EPC]", "Renin Inhibitors [MoA]"], "product_ndc": "49884-425", "generic_name": "ALISKIREN", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALISKIREN", "active_ingredients": [{"name": "ALISKIREN HEMIFUMARATE", "strength": "300 mg/1"}], "application_number": "ANDA206665", "marketing_category": "ANDA", "marketing_start_date": "20190325", "listing_expiration_date": "20261231"}