Package 71205-522-60

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 71205-522-60
Digits Only 7120552260
Product NDC 71205-522
Description

60 TABLET, FILM COATED in 1 BOTTLE (71205-522-60)

Marketing

Marketing Status
Marketed Since 2025-05-19
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": "89d2987c-469d-416c-b81b-70a3fff64427", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0371205522209"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["c5eaa3a9-5aa8-46b0-8cec-639bfb327475"], "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": "20 TABLET, FILM COATED in 1 BOTTLE (71205-522-20)", "package_ndc": "71205-522-20", "marketing_start_date": "20210107"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (71205-522-28)", "package_ndc": "71205-522-28", "marketing_start_date": "20210107"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-522-30)", "package_ndc": "71205-522-30", "marketing_start_date": "20210107"}, {"sample": false, "description": "42 TABLET, FILM COATED in 1 BOTTLE (71205-522-42)", "package_ndc": "71205-522-42", "marketing_start_date": "20240801"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-522-60)", "package_ndc": "71205-522-60", "marketing_start_date": "20250519"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-522-90)", "package_ndc": "71205-522-90", "marketing_start_date": "20250519"}], "brand_name": "Ibuprofen", "product_id": "71205-522_89d2987c-469d-416c-b81b-70a3fff64427", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71205-522", "generic_name": "Ibuprofen", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA078329", "marketing_category": "ANDA", "marketing_start_date": "20180824", "listing_expiration_date": "20261231"}