Package 0615-8309-39

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 0615-8309-39
Digits Only 0615830939
Product NDC 0615-8309
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8309-39)

Marketing

Marketing Status
Marketed Since 2019-07-02
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": "93767828-fe9c-406f-8ad3-dbf225133126", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197805", "197806"], "spl_set_id": ["ab11e142-9e11-4ce4-9671-7e4fe53ffe92"], "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": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8309-39)", "package_ndc": "0615-8309-39", "marketing_start_date": "20190702"}], "brand_name": "Ibuprofen", "product_id": "0615-8309_93767828-fe9c-406f-8ad3-dbf225133126", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0615-8309", "generic_name": "Ibuprofen", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "400 mg/1"}], "application_number": "ANDA078329", "marketing_category": "ANDA", "marketing_start_date": "20140401", "listing_expiration_date": "20261231"}