Package 53746-132-05
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
53746-132-05
Digits Only
5374613205
Product NDC
53746-132
Description
500 TABLET in 1 BOTTLE (53746-132-05)
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": "fc9fc973-31c3-42df-93e7-eeeeb280bcaa", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0353746132017"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["8df77ead-27eb-4f6f-95a9-f68d3e9cfa71"], "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": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (53746-132-01)", "package_ndc": "53746-132-01", "marketing_start_date": "20090105"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (53746-132-05)", "package_ndc": "53746-132-05", "marketing_start_date": "20090105"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (53746-132-30)", "package_ndc": "53746-132-30", "marketing_start_date": "20090105"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (53746-132-50)", "package_ndc": "53746-132-50", "marketing_start_date": "20090105"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (53746-132-60)", "package_ndc": "53746-132-60", "marketing_start_date": "20090105"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (53746-132-90)", "package_ndc": "53746-132-90", "marketing_start_date": "20090105"}], "brand_name": "Ibuprofen", "product_id": "53746-132_fc9fc973-31c3-42df-93e7-eeeeb280bcaa", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "53746-132", "generic_name": "Ibuprofen", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA071335", "marketing_category": "ANDA", "marketing_start_date": "20090105", "listing_expiration_date": "20261231"}