Package 49483-114-73

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 49483-114-73
Digits Only 4948311473
Product NDC 49483-114
Description

100 TABLET, FILM COATED in 1 BOTTLE (49483-114-73)

Marketing

Marketing Status
Marketed Since 2023-11-18
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": "375d8923-4e92-d631-e063-6294a90a20eb", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0349483600018", "0349483601015", "0349483600056", "0349483114171", "0349483600506"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["f58d35f9-e44b-417b-98ce-0766b537cd2f"], "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": "1000 TABLET, FILM COATED in 1 BOTTLE (49483-114-10)", "package_ndc": "49483-114-10", "marketing_start_date": "20210909"}, {"sample": false, "description": "200 TABLET, FILM COATED in 1 BOTTLE (49483-114-17)", "package_ndc": "49483-114-17", "marketing_start_date": "20230819"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (49483-114-50)", "package_ndc": "49483-114-50", "marketing_start_date": "20210909"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (49483-114-73)", "package_ndc": "49483-114-73", "marketing_start_date": "20231118"}], "brand_name": "Ibuprofen", "product_id": "49483-114_375d8923-4e92-d631-e063-6294a90a20eb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "49483-114", "generic_name": "Ibuprofen", "labeler_name": "TIME CAP LABORATORIES,INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA091239", "marketing_category": "ANDA", "marketing_start_date": "20160322", "listing_expiration_date": "20261231"}