Package 70000-0622-2
Brand: acetaminophen and ibuprofen
Generic: acetaminophen and ibuprofenPackage Facts
Identity
Package NDC
70000-0622-2
Digits Only
7000006222
Product NDC
70000-0622
Description
36 TABLET in 1 BOTTLE (70000-0622-2)
Marketing
Marketing Status
Brand
acetaminophen and ibuprofen
Generic
acetaminophen and ibuprofen
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4652fd1e-ed26-2a97-e063-6394a90a7e1a", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["362O9ITL9D", "WK2XYI10QM"], "rxcui": ["2387532"], "spl_set_id": ["f1d69088-4d52-cbb5-e053-2995a90a3ec8"], "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": ["LEADER/ Cardinal Health 110, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "18 TABLET in 1 BOTTLE (70000-0622-1)", "package_ndc": "70000-0622-1", "marketing_start_date": "20230715"}, {"sample": false, "description": "36 TABLET in 1 BOTTLE (70000-0622-2)", "package_ndc": "70000-0622-2", "marketing_start_date": "20230715"}], "brand_name": "Acetaminophen and Ibuprofen", "product_id": "70000-0622_4652fd1e-ed26-2a97-e063-6394a90a7e1a", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70000-0622", "generic_name": "Acetaminophen and Ibuprofen", "labeler_name": "LEADER/ Cardinal Health 110, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen and Ibuprofen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "IBUPROFEN", "strength": "125 mg/1"}], "application_number": "ANDA216592", "marketing_category": "ANDA", "marketing_start_date": "20230715", "listing_expiration_date": "20261231"}