Package 49483-716-49

Brand: dual action pain relief

Generic: acetaminophen, ibuprofen
NDC Package

Package Facts

Identity

Package NDC 49483-716-49
Digits Only 4948371649
Product NDC 49483-716
Product ID 49483-716_08acd3bf-ad0d-f693-e063-6394a90ad8c2
Description

1 BOTTLE in 1 CARTON (49483-716-49) / 144 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2023-10-13
Brand dual action pain relief
Generic acetaminophen, ibuprofen
Sample Package No

Linked Drug Pages (1)

Dual Action Pain Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "08acd3bf-ad0d-f693-e063-6394a90ad8c2", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0349483716757", "0349483716498"], "unii": ["362O9ITL9D", "WK2XYI10QM"], "rxcui": ["2387532"], "spl_set_id": ["08acd3bf-ad0c-f693-e063-6394a90ad8c2"], "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": "1 BOTTLE in 1 CARTON (49483-716-49)  / 144 TABLET in 1 BOTTLE", "package_ndc": "49483-716-49", "marketing_start_date": "20231013"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (49483-716-75)  / 72 TABLET in 1 BOTTLE", "package_ndc": "49483-716-75", "marketing_start_date": "20231013"}], "brand_name": "Dual Action Pain Relief", "product_id": "49483-716_08acd3bf-ad0d-f693-e063-6394a90ad8c2", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "49483-716", "generic_name": "Acetaminophen, Ibuprofen", "labeler_name": "TIME CAP LABORATORIES, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dual Action Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "IBUPROFEN", "strength": "125 mg/1"}], "application_number": "ANDA216994", "marketing_category": "ANDA", "marketing_start_date": "20231013", "listing_expiration_date": "20261231"}