Package 69367-396-01
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
69367-396-01
Digits Only
6936739601
Product NDC
69367-396
Description
100 TABLET, FILM COATED in 1 BOTTLE (69367-396-01)
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": "786c8d96-734d-4905-ae64-490c41bfbf40", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197805", "197806", "197807"], "spl_set_id": ["eeb8312f-7fd9-4c4f-8264-a7e63ff1aa9d"], "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": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69367-396-01)", "package_ndc": "69367-396-01", "marketing_start_date": "20240523"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (69367-396-05)", "package_ndc": "69367-396-05", "marketing_start_date": "20240523"}], "brand_name": "Ibuprofen", "product_id": "69367-396_786c8d96-734d-4905-ae64-490c41bfbf40", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69367-396", "generic_name": "Ibuprofen", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA202413", "marketing_category": "ANDA", "marketing_start_date": "20240523", "listing_expiration_date": "20261231"}