Package 50580-409-12
Brand: motrin ib
Generic: ibuprofenPackage Facts
Identity
Package NDC
50580-409-12
Digits Only
5058040912
Product NDC
50580-409
Description
1 BOTTLE, PLASTIC in 1 CARTON (50580-409-12) / 120 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
Marketing
Marketing Status
Brand
motrin ib
Generic
ibuprofen
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "460ce926-0d5f-b418-e063-6394a90a74ce", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0300450409201"], "unii": ["WK2XYI10QM"], "rxcui": ["310964", "606990"], "spl_set_id": ["d9fc716a-fba5-45f8-8024-52325799d1dd"], "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": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50580-409-12) / 120 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC", "package_ndc": "50580-409-12", "marketing_start_date": "20150126"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50580-409-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC", "package_ndc": "50580-409-20", "marketing_start_date": "20150126"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50580-409-80) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC", "package_ndc": "50580-409-80", "marketing_start_date": "20150126"}], "brand_name": "Motrin IB", "product_id": "50580-409_460ce926-0d5f-b418-e063-6394a90a74ce", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50580-409", "generic_name": "Ibuprofen", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Motrin IB", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA078682", "marketing_category": "ANDA", "marketing_start_date": "20150126", "listing_expiration_date": "20261231"}