Package 70518-1409-0

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 70518-1409-0
Digits Only 7051814090
Product NDC 70518-1409
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1409-0)

Marketing

Marketing Status
Marketed Since 2018-09-11
Brand ibuprofen
Generic ibuprofen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48fc9ffa-555c-2799-e063-6394a90a67d0", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197807"], "spl_set_id": ["421156d2-85dc-4680-b2b4-d15b67539e87"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1409-0)", "package_ndc": "70518-1409-0", "marketing_start_date": "20180911"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BLISTER PACK (70518-1409-1)", "package_ndc": "70518-1409-1", "marketing_start_date": "20180914"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1409-2)", "package_ndc": "70518-1409-2", "marketing_start_date": "20180917"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1409-4)", "package_ndc": "70518-1409-4", "marketing_start_date": "20180924"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BLISTER PACK (70518-1409-5)", "package_ndc": "70518-1409-5", "marketing_start_date": "20181008"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1409-9)", "package_ndc": "70518-1409-9", "marketing_start_date": "20210520"}], "brand_name": "Ibuprofen", "product_id": "70518-1409_48fc9ffa-555c-2799-e063-6394a90a67d0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70518-1409", "generic_name": "Ibuprofen", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA091625", "marketing_category": "ANDA", "marketing_start_date": "20180911", "listing_expiration_date": "20271231"}