Package 60760-604-90

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 60760-604-90
Digits Only 6076060490
Product NDC 60760-604
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-604-90)

Marketing

Marketing Status
Marketed Since 2019-10-16
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": "292d2188-34d5-ef2f-e063-6394a90ad014", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197807"], "spl_set_id": ["950c3ca7-4481-976f-e053-2995a90ad51e"], "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": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-604-09)", "package_ndc": "60760-604-09", "marketing_start_date": "20200610"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-604-20)", "package_ndc": "60760-604-20", "marketing_start_date": "20191016"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-604-30)", "package_ndc": "60760-604-30", "marketing_start_date": "20200708"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-604-60)", "package_ndc": "60760-604-60", "marketing_start_date": "20191016"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-604-90)", "package_ndc": "60760-604-90", "marketing_start_date": "20191016"}], "brand_name": "IBUPROFEN", "product_id": "60760-604_292d2188-34d5-ef2f-e063-6394a90ad014", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "60760-604", "generic_name": "IBUPROFEN", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IBUPROFEN", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA090796", "marketing_category": "ANDA", "marketing_start_date": "20191016", "listing_expiration_date": "20261231"}