Package 71205-604-40

Brand: ibu

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 71205-604-40
Digits Only 7120560440
Product NDC 71205-604
Description

40 TABLET in 1 BOTTLE (71205-604-40)

Marketing

Marketing Status
Marketed Since 2021-09-27
Brand ibu
Generic ibuprofen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f49b4e82-120c-4012-b4b3-78c0f89ae8fd", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0371205604158"], "unii": ["WK2XYI10QM"], "spl_set_id": ["ea6f626d-cda3-46e2-9ac9-4e72204cb726"], "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": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (71205-604-15)", "package_ndc": "71205-604-15", "marketing_start_date": "20210927"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71205-604-20)", "package_ndc": "71205-604-20", "marketing_start_date": "20210927"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (71205-604-21)", "package_ndc": "71205-604-21", "marketing_start_date": "20210927"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-604-30)", "package_ndc": "71205-604-30", "marketing_start_date": "20210827"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71205-604-40)", "package_ndc": "71205-604-40", "marketing_start_date": "20210927"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-604-60)", "package_ndc": "71205-604-60", "marketing_start_date": "20210827"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-604-90)", "package_ndc": "71205-604-90", "marketing_start_date": "20210827"}], "brand_name": "IBU", "product_id": "71205-604_f49b4e82-120c-4012-b4b3-78c0f89ae8fd", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71205-604", "generic_name": "Ibuprofen", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IBU", "active_ingredients": [{"name": "IBUPROFEN", "strength": "400 mg/1"}], "application_number": "ANDA075682", "marketing_category": "ANDA", "marketing_start_date": "20081120", "listing_expiration_date": "20261231"}