Package 68788-8438-2
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
68788-8438-2
Digits Only
6878884382
Product NDC
68788-8438
Description
20 TABLET in 1 BOTTLE (68788-8438-2)
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": "3df8bc00-5b35-420f-b3c5-30b40c93c82c", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197805"], "spl_set_id": ["bdc3f482-6fba-4420-9118-0f5cb7744e97"], "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": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8438-1)", "package_ndc": "68788-8438-1", "marketing_start_date": "20230428"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68788-8438-2)", "package_ndc": "68788-8438-2", "marketing_start_date": "20230428"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8438-3)", "package_ndc": "68788-8438-3", "marketing_start_date": "20230428"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (68788-8438-5)", "package_ndc": "68788-8438-5", "marketing_start_date": "20230428"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8438-6)", "package_ndc": "68788-8438-6", "marketing_start_date": "20230428"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (68788-8438-8)", "package_ndc": "68788-8438-8", "marketing_start_date": "20230428"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8438-9)", "package_ndc": "68788-8438-9", "marketing_start_date": "20230428"}], "brand_name": "Ibuprofen", "product_id": "68788-8438_3df8bc00-5b35-420f-b3c5-30b40c93c82c", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-8438", "generic_name": "Ibuprofen", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "400 mg/1"}], "application_number": "ANDA213794", "marketing_category": "ANDA", "marketing_start_date": "20230428", "listing_expiration_date": "20261231"}