Package 70518-0005-6

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 70518-0005-6
Digits Only 7051800056
Product NDC 70518-0005
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0005-6)

Marketing

Marketing Status
Marketed Since 2023-03-17
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": "4cc5a30b-25f6-d6fd-e063-6394a90a4cc1", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "spl_set_id": ["9dfc752f-3f66-4c39-bfa8-db6de9a9a9bf"], "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 BLISTER PACK (70518-0005-6)", "package_ndc": "70518-0005-6", "marketing_start_date": "20230317"}], "brand_name": "IBUPROFEN", "product_id": "70518-0005_4cc5a30b-25f6-d6fd-e063-6394a90a4cc1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70518-0005", "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": "ANDA090796", "marketing_category": "ANDA", "marketing_start_date": "20161117", "listing_expiration_date": "20271231"}