Package 53746-143-24

Brand: ibuprofen pain releiver/ fever reducer

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 53746-143-24
Digits Only 5374614324
Product NDC 53746-143
Description

24 TABLET in 1 BOTTLE (53746-143-24)

Marketing

Marketing Status
Marketed Since 2009-12-16
Brand ibuprofen pain releiver/ fever reducer
Generic ibuprofen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e2b9bf54-0449-4f9b-86e8-e3b292387dd5", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0353746144249"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["ee241be0-35f8-4789-a71f-98de31d6a590"], "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 (53746-143-01)", "package_ndc": "53746-143-01", "marketing_start_date": "20091216"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (53746-143-10)", "package_ndc": "53746-143-10", "marketing_start_date": "20091216"}, {"sample": false, "description": "24 TABLET in 1 BOTTLE (53746-143-24)", "package_ndc": "53746-143-24", "marketing_start_date": "20091216"}], "brand_name": "Ibuprofen Pain Releiver/ Fever Reducer", "product_id": "53746-143_e2b9bf54-0449-4f9b-86e8-e3b292387dd5", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "53746-143", "generic_name": "Ibuprofen", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "brand_name_suffix": "Pain Releiver/ Fever Reducer", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA071333", "marketing_category": "ANDA", "marketing_start_date": "20091216", "listing_expiration_date": "20261231"}