Package 59726-046-20

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 59726-046-20
Digits Only 5972604620
Product NDC 59726-046
Description

1 BOTTLE, PLASTIC in 1 BOX (59726-046-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2027-02-01
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": "0cccdcc0-9b0b-434e-b693-82924b44f3d9", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0359726745062"], "unii": ["WK2XYI10QM"], "rxcui": ["310964"], "spl_set_id": ["ce215099-91b0-43fd-8ac9-17fe6508842c"], "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": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "160 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (59726-046-16)", "package_ndc": "59726-046-16", "marketing_end_date": "20270201", "marketing_start_date": "20201204"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-046-20)  / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC", "package_ndc": "59726-046-20", "marketing_end_date": "20270201", "marketing_start_date": "20201204"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-046-30)  / 30 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC", "package_ndc": "59726-046-30", "marketing_end_date": "20270201", "marketing_start_date": "20201204"}], "brand_name": "Ibuprofen", "product_id": "59726-046_0cccdcc0-9b0b-434e-b693-82924b44f3d9", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "59726-046", "generic_name": "Ibuprofen", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA207753", "marketing_category": "ANDA", "marketing_end_date": "20270201", "marketing_start_date": "20201204"}