Package 50090-5819-0

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 50090-5819-0
Digits Only 5009058190
Product NDC 50090-5819
Description

16 TABLET, FILM COATED in 1 BOTTLE (50090-5819-0)

Marketing

Marketing Status
Marketed Since 2021-10-19
Brand ibuprofen
Generic ibuprofen
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "928aea26-2b55-4e1c-9a7d-9aeddfdb32a5", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197805"], "spl_set_id": ["400faee1-f662-470e-bcd6-7711dfaf9ba2"], "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": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "16 TABLET, FILM COATED in 1 BOTTLE (50090-5819-0)", "package_ndc": "50090-5819-0", "marketing_start_date": "20211019"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-5819-1)", "package_ndc": "50090-5819-1", "marketing_start_date": "20211019"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-5819-3)", "package_ndc": "50090-5819-3", "marketing_start_date": "20211019"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-5819-4)", "package_ndc": "50090-5819-4", "marketing_start_date": "20211019"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-5819-8)", "package_ndc": "50090-5819-8", "marketing_start_date": "20211019"}], "brand_name": "Ibuprofen", "product_id": "50090-5819_928aea26-2b55-4e1c-9a7d-9aeddfdb32a5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50090-5819", "generic_name": "Ibuprofen", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "400 mg/1"}], "application_number": "ANDA078329", "marketing_category": "ANDA", "marketing_start_date": "20180824", "listing_expiration_date": "20261231"}