Package 41163-103-68

Brand: equaline dual action pain reliever

Generic: acetaminophen, ibuprofen
NDC Package

Package Facts

Identity

Package NDC 41163-103-68
Digits Only 4116310368
Product NDC 41163-103
Product ID 41163-103_4348c154-9502-40c5-84d1-816ccd1ac90f
Description

1 BOTTLE in 1 CARTON (41163-103-68) / 36 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-03-21
Brand equaline dual action pain reliever
Generic acetaminophen, ibuprofen
Sample Package No

Linked Drug Pages (1)

equaline dual action pain reliever ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4348c154-9502-40c5-84d1-816ccd1ac90f", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["362O9ITL9D", "WK2XYI10QM"], "rxcui": ["2387532"], "spl_set_id": ["ae0dc3f1-ee6f-4347-af5d-70f45dd68bdb"], "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": ["United Natural Foods, Inc. dba UNFI"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (41163-103-68)  / 36 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41163-103-68", "marketing_start_date": "20240321"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41163-103-89)  / 18 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41163-103-89", "marketing_start_date": "20240321"}], "brand_name": "equaline dual action pain reliever", "product_id": "41163-103_4348c154-9502-40c5-84d1-816ccd1ac90f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "41163-103", "generic_name": "Acetaminophen, Ibuprofen", "labeler_name": "United Natural Foods, Inc. dba UNFI", "product_type": "HUMAN OTC DRUG", "brand_name_base": "equaline dual action pain reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "IBUPROFEN", "strength": "125 mg/1"}], "application_number": "ANDA214836", "marketing_category": "ANDA", "marketing_start_date": "20240321", "listing_expiration_date": "20261231"}