Package 0904-6747-40
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
0904-6747-40
Digits Only
0904674740
Product NDC
0904-6747
Description
500 TABLET, FILM COATED in 1 BOTTLE (0904-6747-40)
Marketing
Marketing Status
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"}