Package 41250-604-90

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 41250-604-90
Digits Only 4125060490
Product NDC 41250-604
Description

500 TABLET, FILM COATED in 1 BOTTLE (41250-604-90)

Marketing

Marketing Status
Marketed Since 1992-05-22
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": "4e6148c7-fafa-4303-bc95-1dc96dee075d", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["e578de96-747e-4104-8db6-e6521e6052a5"], "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": ["Meijer Distribution Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (41250-604-62)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41250-604-62", "marketing_start_date": "19940907"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41250-604-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41250-604-71", "marketing_start_date": "19880215"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41250-604-78)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41250-604-78", "marketing_start_date": "19901215"}, {"sample": false, "description": "2 BOTTLE in 1 CARTON (41250-604-82)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41250-604-82", "marketing_start_date": "20110513"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (41250-604-90)", "package_ndc": "41250-604-90", "marketing_start_date": "19920522"}], "brand_name": "ibuprofen", "product_id": "41250-604_4e6148c7-fafa-4303-bc95-1dc96dee075d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "41250-604", "generic_name": "Ibuprofen", "labeler_name": "Meijer Distribution Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA072096", "marketing_category": "ANDA", "marketing_start_date": "19880215", "listing_expiration_date": "20261231"}