Package 68071-5066-4

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 68071-5066-4
Digits Only 6807150664
Product NDC 68071-5066
Description

4 TABLET, FILM COATED in 1 BOTTLE (68071-5066-4)

Marketing

Marketing Status
Marketed Since 2019-09-19
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": "1c5cd5d2-aa5a-5acf-e063-6394a90a3414", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0368071506648"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["92efad86-31ae-78e5-e053-2995a90a0fda"], "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": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (68071-5066-4)", "package_ndc": "68071-5066-4", "marketing_start_date": "20190919"}], "brand_name": "Ibuprofen", "product_id": "68071-5066_1c5cd5d2-aa5a-5acf-e063-6394a90a3414", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68071-5066", "generic_name": "Ibuprofen", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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": "20140401", "listing_expiration_date": "20261231"}