Package 41250-647-78

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 41250-647-78
Digits Only 4125064778
Product NDC 41250-647
Description

1 BOTTLE in 1 CARTON (41250-647-78) / 100 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 1991-09-20
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": "27661b00-42d1-4f86-8c56-04cfece82d4f", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["66b19ed1-6cf9-4705-82cd-02f23c6379e7"], "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 (41250-647-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41250-647-71", "marketing_start_date": "19881115"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41250-647-78)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41250-647-78", "marketing_start_date": "19910920"}, {"sample": false, "description": "2 BOTTLE in 1 CARTON (41250-647-82)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41250-647-82", "marketing_start_date": "20160902"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (41250-647-90)", "package_ndc": "41250-647-90", "marketing_start_date": "19940907"}], "brand_name": "ibuprofen", "product_id": "41250-647_27661b00-42d1-4f86-8c56-04cfece82d4f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "41250-647", "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": "19881115", "listing_expiration_date": "20261231"}