Package 0904-7588-59
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
0904-7588-59
Digits Only
0904758859
Product NDC
0904-7588
Description
100 TABLET, FILM COATED in 1 BOTTLE (0904-7588-59)
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": "4a1aa866-e39a-68e6-e063-6394a90a6432", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197805", "197806", "197807"], "spl_set_id": ["42b6faf5-ef47-6a7a-e063-6394a90ac409"], "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": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (0904-7588-40)", "package_ndc": "0904-7588-40", "marketing_start_date": "20251103"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0904-7588-59)", "package_ndc": "0904-7588-59", "marketing_start_date": "20251103"}], "brand_name": "Ibuprofen", "product_id": "0904-7588_4a1aa866-e39a-68e6-e063-6394a90a6432", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0904-7588", "generic_name": "Ibuprofen", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA071268", "marketing_category": "ANDA", "marketing_start_date": "20251103", "listing_expiration_date": "20271231"}