Package 80425-0132-3
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
80425-0132-3
Digits Only
8042501323
Product NDC
80425-0132
Description
90 TABLET, FILM COATED in 1 BOTTLE (80425-0132-3)
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": "2a99c0c8-93b9-9e14-e063-6394a90a332b", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["bd1ca7af-d640-23fb-e053-2a95a90a8a98"], "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": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0132-1)", "package_ndc": "80425-0132-1", "marketing_start_date": "20151230"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0132-2)", "package_ndc": "80425-0132-2", "marketing_start_date": "20151230"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0132-3)", "package_ndc": "80425-0132-3", "marketing_start_date": "20151230"}], "brand_name": "Ibuprofen", "product_id": "80425-0132_2a99c0c8-93b9-9e14-e063-6394a90a332b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "80425-0132", "generic_name": "Ibuprofen", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA090796", "marketing_category": "ANDA", "marketing_start_date": "20151230", "listing_expiration_date": "20261231"}