Package 11673-993-26
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
11673-993-26
Digits Only
1167399326
Product NDC
11673-993
Description
225 TABLET, COATED in 1 BOTTLE (11673-993-26)
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": "0e07c84c-691d-97b3-e063-6394a90aa81d", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0349483612264"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["8e872c8d-28e2-cd49-e053-2995a90a469f"], "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": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (11673-993-01)", "package_ndc": "11673-993-01", "marketing_start_date": "20200101"}, {"sample": false, "description": "225 TABLET, COATED in 1 BOTTLE (11673-993-26)", "package_ndc": "11673-993-26", "marketing_start_date": "20200101"}], "brand_name": "IBUPROFEN", "product_id": "11673-993_0e07c84c-691d-97b3-e063-6394a90aa81d", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11673-993", "generic_name": "IBUPROFEN", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "IBUPROFEN", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA091237", "marketing_category": "ANDA", "marketing_start_date": "20200101", "listing_expiration_date": "20261231"}