Package 65162-770-11
Brand: ibuprofen pain reliever/fever reducer
Generic: ibuprofenPackage Facts
Identity
Package NDC
65162-770-11
Digits Only
6516277011
Product NDC
65162-770
Description
1000 CAPSULE, LIQUID FILLED in 1 BOTTLE (65162-770-11)
Marketing
Marketing Status
Brand
ibuprofen pain reliever/fever reducer
Generic
ibuprofen
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7eec8df5-4a15-47be-9031-3e046204d452", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310964"], "spl_set_id": ["5f27dd3f-c735-417b-95e6-26dc5aae5a7a"], "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": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (65162-770-02) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE", "package_ndc": "65162-770-02", "marketing_start_date": "20111223"}, {"sample": false, "description": "1000 CAPSULE, LIQUID FILLED in 1 BOTTLE (65162-770-11)", "package_ndc": "65162-770-11", "marketing_start_date": "20111223"}, {"sample": false, "description": "500 CAPSULE, LIQUID FILLED in 1 BOTTLE (65162-770-50)", "package_ndc": "65162-770-50", "marketing_start_date": "20111223"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (65162-770-69) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE", "package_ndc": "65162-770-69", "marketing_start_date": "20111223"}], "brand_name": "Ibuprofen Pain Reliever/Fever Reducer", "product_id": "65162-770_7eec8df5-4a15-47be-9031-3e046204d452", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "65162-770", "generic_name": "Ibuprofen", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen Pain Reliever/Fever Reducer", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA202300", "marketing_category": "ANDA", "marketing_start_date": "20111223", "listing_expiration_date": "20261231"}