Package 49483-603-05
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
49483-603-05
Digits Only
4948360305
Product NDC
49483-603
Description
50 TABLET, FILM COATED in 1 BOTTLE (49483-603-05)
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": "27b8b074-c62d-7214-e063-6294a90adb69", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0349483604504", "0349483604016", "0349483602012", "0349483602500", "0349483603507", "0349483603019"], "unii": ["WK2XYI10QM"], "rxcui": ["197805", "197806", "197807"], "spl_set_id": ["ec3e8443-d742-4c25-8516-f0df4ebfccdc"], "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": ["TIME CAP LABORATORIES, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (49483-603-01)", "package_ndc": "49483-603-01", "marketing_start_date": "20151230"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (49483-603-03)", "package_ndc": "49483-603-03", "marketing_start_date": "20151230"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (49483-603-05)", "package_ndc": "49483-603-05", "marketing_start_date": "20151230"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (49483-603-50)", "package_ndc": "49483-603-50", "marketing_start_date": "20151230"}], "brand_name": "Ibuprofen", "product_id": "49483-603_27b8b074-c62d-7214-e063-6294a90adb69", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "49483-603", "generic_name": "Ibuprofen", "labeler_name": "TIME CAP LABORATORIES, INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA090796", "marketing_category": "ANDA", "marketing_start_date": "20151230", "listing_expiration_date": "20261231"}