Package 80425-0154-1

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 80425-0154-1
Digits Only 8042501541
Product NDC 80425-0154
Description

30 TABLET, FILM COATED in 1 BOTTLE (80425-0154-1)

Marketing

Marketing Status
Marketed Since 2015-12-21
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": "2a99a80e-d06d-27e6-e063-6294a90ae0fe", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["c859cc7a-e13a-7df4-e053-2a95a90a47d6"], "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": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0154-1)", "package_ndc": "80425-0154-1", "marketing_start_date": "20151221"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0154-2)", "package_ndc": "80425-0154-2", "marketing_start_date": "20151221"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0154-3)", "package_ndc": "80425-0154-3", "marketing_start_date": "20151221"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (80425-0154-4)", "package_ndc": "80425-0154-4", "marketing_start_date": "20230516"}], "brand_name": "Ibuprofen", "product_id": "80425-0154_2a99a80e-d06d-27e6-e063-6294a90ae0fe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "80425-0154", "generic_name": "Ibuprofen", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA091625", "marketing_category": "ANDA", "marketing_start_date": "20151221", "listing_expiration_date": "20261231"}