Package 70518-1364-7
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
70518-1364-7
Digits Only
7051813647
Product NDC
70518-1364
Description
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1364-7)
Marketing
Marketing Status
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": "48e95346-8f79-49bf-e063-6394a90abdec", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["b6a6c940-daf6-4e0e-aefb-35cce87a9a55"], "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": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1364-2)", "package_ndc": "70518-1364-2", "marketing_start_date": "20201023"}, {"sample": false, "description": "27 TABLET, FILM COATED in 1 BLISTER PACK (70518-1364-4)", "package_ndc": "70518-1364-4", "marketing_start_date": "20230730"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1364-5)", "package_ndc": "70518-1364-5", "marketing_start_date": "20230802"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1364-7)", "package_ndc": "70518-1364-7", "marketing_start_date": "20250429"}, {"sample": false, "description": "100 POUCH in 1 BOX (70518-1364-8) / 1 TABLET, FILM COATED in 1 POUCH (70518-1364-9)", "package_ndc": "70518-1364-8", "marketing_start_date": "20251205"}], "brand_name": "Ibuprofen", "product_id": "70518-1364_48e95346-8f79-49bf-e063-6394a90abdec", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70518-1364", "generic_name": "Ibuprofen", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA091625", "marketing_category": "ANDA", "marketing_start_date": "20180809", "listing_expiration_date": "20271231"}