Package 76420-415-60

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 76420-415-60
Digits Only 7642041560
Product NDC 76420-415
Description

60 TABLET in 1 BOTTLE (76420-415-60)

Marketing

Marketing Status
Marketed Since 2025-08-02
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": "3b5c08ee-3c0c-616f-e063-6394a90a379a", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197807"], "spl_set_id": ["d7ed42c4-371c-4a54-ab15-0630656f0427"], "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": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-415-01)", "package_ndc": "76420-415-01", "marketing_start_date": "20250802"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (76420-415-05)", "package_ndc": "76420-415-05", "marketing_start_date": "20250802"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-415-30)", "package_ndc": "76420-415-30", "marketing_start_date": "20250802"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-415-60)", "package_ndc": "76420-415-60", "marketing_start_date": "20250802"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-415-90)", "package_ndc": "76420-415-90", "marketing_start_date": "20250802"}], "brand_name": "Ibuprofen", "product_id": "76420-415_3b5c08ee-3c0c-616f-e063-6394a90a379a", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "76420-415", "generic_name": "ibuprofen", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA078329", "marketing_category": "ANDA", "marketing_start_date": "20241201", "listing_expiration_date": "20261231"}