Package 0078-0568-45

Brand: coartem

Generic: artemether and lumefantrine
NDC Package

Package Facts

Identity

Package NDC 0078-0568-45
Digits Only 0078056845
Product NDC 0078-0568
Product ID 0078-0568_3890be50-58ca-4301-91c4-5e8ab19923ad
Description

24 TABLET in 1 BOTTLE (0078-0568-45)

Marketing

Marketing Status
Marketed Since 2009-04-07
Brand coartem
Generic artemether and lumefantrine
Sample Package No

Linked Drug Pages (1)

COARTEM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3890be50-58ca-4301-91c4-5e8ab19923ad", "openfda": {"nui": ["N0000175482"], "unii": ["C7D6T3H22J", "F38R0JR742"], "rxcui": ["847731", "847734"], "spl_set_id": ["7866ec19-dfac-47d4-a53f-511a12643cbf"], "pharm_class_epc": ["Antimalarial [EPC]"], "manufacturer_name": ["Novartis Pharmaceuticals Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 TABLET in 1 BOTTLE (0078-0568-45)", "package_ndc": "0078-0568-45", "marketing_start_date": "20090407"}], "brand_name": "COARTEM", "product_id": "0078-0568_3890be50-58ca-4301-91c4-5e8ab19923ad", "dosage_form": "TABLET", "pharm_class": ["Antimalarial [EPC]", "Antimalarial [EPC]"], "product_ndc": "0078-0568", "generic_name": "artemether and lumefantrine", "labeler_name": "Novartis Pharmaceuticals Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "COARTEM", "active_ingredients": [{"name": "ARTEMETHER", "strength": "20 mg/1"}, {"name": "LUMEFANTRINE", "strength": "120 mg/1"}], "application_number": "NDA022268", "marketing_category": "NDA", "marketing_start_date": "20090407", "listing_expiration_date": "20261231"}