Package 50090-2996-1

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 50090-2996-1
Digits Only 5009029961
Product NDC 50090-2996
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-2996-1)

Marketing

Marketing Status
Marketed Since 2017-05-10
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": "f0c4785a-b0fb-439c-b323-1fa74881a338", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197805", "197806", "197807"], "spl_set_id": ["51de1183-d226-4869-a00a-f6c74e126a39"], "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 (50090-2996-0)", "package_ndc": "50090-2996-0", "marketing_start_date": "20170907"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-2996-1)", "package_ndc": "50090-2996-1", "marketing_start_date": "20170510"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-2996-3)", "package_ndc": "50090-2996-3", "marketing_start_date": "20170508"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-2996-4)", "package_ndc": "50090-2996-4", "marketing_start_date": "20170502"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-2996-8)", "package_ndc": "50090-2996-8", "marketing_start_date": "20170807"}], "brand_name": "Ibuprofen", "product_id": "50090-2996_f0c4785a-b0fb-439c-b323-1fa74881a338", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50090-2996", "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": "ANDA091625", "marketing_category": "ANDA", "marketing_start_date": "20151221", "listing_expiration_date": "20261231"}