Package 71610-892-53

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 71610-892-53
Digits Only 7161089253
Product NDC 71610-892
Description

60 TABLET in 1 BOTTLE (71610-892-53)

Marketing

Marketing Status
Marketed Since 2025-03-28
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": "31e6b2f1-509c-e921-e063-6394a90a2f3c", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197807"], "spl_set_id": ["31e6ac7a-fa3e-4dd4-e063-6294a90a29af"], "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": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (71610-892-53)", "package_ndc": "71610-892-53", "marketing_start_date": "20250328"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-892-60)", "package_ndc": "71610-892-60", "marketing_start_date": "20250328"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71610-892-70)", "package_ndc": "71610-892-70", "marketing_start_date": "20250328"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71610-892-80)", "package_ndc": "71610-892-80", "marketing_start_date": "20250328"}, {"sample": false, "description": "270 TABLET in 1 BOTTLE (71610-892-92)", "package_ndc": "71610-892-92", "marketing_start_date": "20250328"}], "brand_name": "Ibuprofen", "product_id": "71610-892_31e6b2f1-509c-e921-e063-6394a90a2f3c", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71610-892", "generic_name": "Ibuprofen", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA075682", "marketing_category": "ANDA", "marketing_start_date": "20090610", "listing_expiration_date": "20261231"}