Package 53746-144-10
Brand: ibuprofen (nsaid) pain releiver/ fever reducer
Generic: ibuprofenPackage Facts
Identity
Package NDC
53746-144-10
Digits Only
5374614410
Product NDC
53746-144
Description
1000 TABLET in 1 BOTTLE (53746-144-10)
Marketing
Marketing Status
Brand
ibuprofen (nsaid) 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": "ef67c08a-fc4f-4e6c-a58f-8ed743b2b6aa", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0353746142245", "0353746144249"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["a8c6bc4e-1e48-4613-8cbf-8c5cd9d51ad0"], "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 (53746-144-01)", "package_ndc": "53746-144-01", "marketing_start_date": "20091216"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (53746-144-10)", "package_ndc": "53746-144-10", "marketing_start_date": "20091216"}, {"sample": false, "description": "24 TABLET in 1 BOTTLE (53746-144-24)", "package_ndc": "53746-144-24", "marketing_start_date": "20091216"}], "brand_name": "Ibuprofen (NSAID) Pain Releiver/ Fever Reducer", "product_id": "53746-144_ef67c08a-fc4f-4e6c-a58f-8ed743b2b6aa", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "53746-144", "generic_name": "Ibuprofen", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "brand_name_suffix": "(NSAID) Pain Releiver/ Fever Reducer", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA072199", "marketing_category": "ANDA", "marketing_start_date": "20091216", "listing_expiration_date": "20261231"}