Package 0904-6747-59

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 0904-6747-59
Digits Only 0904674759
Product NDC 0904-6747
Description

1 BOTTLE in 1 CARTON (0904-6747-59) / 100 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2018-09-20
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": "dddfc800-cfd3-42d4-82e1-04414822fbfc", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["14f43c32-0895-4ef2-aa54-52b952d058fd"], "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": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0904-6747-24)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0904-6747-24", "marketing_start_date": "20180920"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (0904-6747-40)", "package_ndc": "0904-6747-40", "marketing_start_date": "20180920"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0904-6747-51)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0904-6747-51", "marketing_start_date": "20180920"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0904-6747-59)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0904-6747-59", "marketing_start_date": "20180920"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0904-6747-70)  / 250 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0904-6747-70", "marketing_start_date": "20180920"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (0904-6747-80)", "package_ndc": "0904-6747-80", "marketing_start_date": "20180920"}], "brand_name": "ibuprofen", "product_id": "0904-6747_dddfc800-cfd3-42d4-82e1-04414822fbfc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0904-6747", "generic_name": "Ibuprofen", "labeler_name": "Major Pharmaceuticals", "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": "20180920", "listing_expiration_date": "20261231"}