Package 50580-563-20
Brand: motrin pm
Generic: ibuprofen and diphenhydramine citratePackage Facts
Identity
Package NDC
50580-563-20
Digits Only
5058056320
Product NDC
50580-563
Description
1 BOTTLE, PLASTIC in 1 CARTON (50580-563-20) / 20 TABLET, COATED in 1 BOTTLE, PLASTIC
Marketing
Marketing Status
Brand
motrin pm
Generic
ibuprofen and diphenhydramine citrate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "39a34ab2-9fae-444e-e063-6294a90a9152", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0300450563804"], "unii": ["4OD433S209", "WK2XYI10QM"], "rxcui": ["895664", "895666"], "spl_set_id": ["55403f19-58ae-450b-8a7b-0bc544088f20"], "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 (50580-563-20) / 20 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50580-563-20", "marketing_start_date": "20100111"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50580-563-80) / 80 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50580-563-80", "marketing_start_date": "20100111"}], "brand_name": "Motrin PM", "product_id": "50580-563_39a34ab2-9fae-444e-e063-6294a90a9152", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50580-563", "generic_name": "Ibuprofen and Diphenhydramine Citrate", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Motrin", "brand_name_suffix": "PM", "active_ingredients": [{"name": "DIPHENHYDRAMINE CITRATE", "strength": "38 mg/1"}, {"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA079113", "marketing_category": "ANDA", "marketing_start_date": "20100111", "listing_expiration_date": "20261231"}