Package 43063-914-30
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
43063-914-30
Digits Only
4306391430
Product NDC
43063-914
Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-914-30)
Marketing
Marketing Status
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": "2b9876fb-e9e3-4dbc-e063-6294a90a8696", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0343063914304"], "unii": ["WK2XYI10QM"], "rxcui": ["197807"], "spl_set_id": ["7546e868-d99f-4f8c-b1e9-cc96fd9fa1eb"], "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": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-914-30)", "package_ndc": "43063-914-30", "marketing_start_date": "20181213"}], "brand_name": "Ibuprofen", "product_id": "43063-914_2b9876fb-e9e3-4dbc-e063-6294a90a8696", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "43063-914", "generic_name": "Ibuprofen", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "20151230", "listing_expiration_date": "20261231"}