Package 83615-0001-3
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
83615-0001-3
Digits Only
8361500013
Product NDC
83615-0001
Description
30 TABLET, FILM COATED in 1 BOTTLE (83615-0001-3)
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": "b03fb995-0ee7-4043-b6cb-8e5a444d3d62", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["894a5d14-e405-43ac-a5a2-0b4de5b28474"], "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": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (83615-0001-3)", "package_ndc": "83615-0001-3", "marketing_start_date": "20230823"}], "brand_name": "Ibuprofen", "product_id": "83615-0001_b03fb995-0ee7-4043-b6cb-8e5a444d3d62", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "83615-0001", "generic_name": "Ibuprofen", "labeler_name": "Bryant Ranch Prepack", "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": "20151221", "listing_expiration_date": "20261231"}