Package 70518-0761-0
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
70518-0761-0
Digits Only
7051807610
Product NDC
70518-0761
Description
20 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-0)
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": "4833d6f7-b039-b892-e063-6394a90ae2a8", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["1e6f3ce7-e8a3-40e8-8437-523ef5277b2e"], "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 BLISTER PACK (70518-0761-0)", "package_ndc": "70518-0761-0", "marketing_start_date": "20171006"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-1)", "package_ndc": "70518-0761-1", "marketing_start_date": "20171006"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-2)", "package_ndc": "70518-0761-2", "marketing_start_date": "20180726"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-3)", "package_ndc": "70518-0761-3", "marketing_start_date": "20180727"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-4)", "package_ndc": "70518-0761-4", "marketing_start_date": "20180730"}], "brand_name": "Ibuprofen", "product_id": "70518-0761_4833d6f7-b039-b892-e063-6394a90ae2a8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70518-0761", "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": "20171006", "listing_expiration_date": "20271231"}